

Hello.
The coordinate HGVS term from ClinVar (NM_001366028.2(DNAH12):c.10778) is based on the hg38 variant position, not hg19. While the transcript mRNA sequence (NM_001366028.2) is the same, the exon boundaries can differ between the assemblies.
You can see the same variant on hg38 matching the correct coordinate here: https://genome.ucsc.edu/s/Lou/RM36776
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