Canonical Allele Identifier: CA378040536
Gene: CALHM1 HGNC NCBI

Linked Data

COSMIC: COSM73996
MyVariant Identifiers: chr10:g.105218165A>C (hg19) chr10:g.103458408A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103458408A>C , CM000672.2:g.103458408A>C GRCh38
NC_000010.10:g.105218165A>C , CM000672.1:g.105218165A>C GRCh37
NC_000010.9:g.105208155A>C NCBI36
NG_016855.1:g.5484T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000329905.6:c.344T>G MANE Select ENSP00000329926.6:p.Val115Gly
ENST00000329905.5:c.344T>G ENSP00000329926.5:p.Val115Gly
NM_001001412.3:c.344T>G NP_001001412.3:p.Val115Gly
NM_001001412.4:c.344T>G MANE Select NP_001001412.3:p.Val115Gly
Search 100 bp 5'
Search 100 bp 3'