Canonical Allele Identifier: CA378040557
Gene: CALHM1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.105218175C>A (hg19) chr10:g.103458418C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103458418C>A , CM000672.2:g.103458418C>A GRCh38
NC_000010.10:g.105218175C>A , CM000672.1:g.105218175C>A GRCh37
NC_000010.9:g.105208165C>A NCBI36
NG_016855.1:g.5474G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000329905.6:c.334G>T MANE Select ENSP00000329926.6:p.Val112Phe
ENST00000329905.5:c.334G>T ENSP00000329926.5:p.Val112Phe
NM_001001412.3:c.334G>T NP_001001412.3:p.Val112Phe
NM_001001412.4:c.334G>T MANE Select NP_001001412.3:p.Val112Phe
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