Canonical Allele Identifier: CA5674692
Gene: CALHM1 HGNC NCBI

Linked Data

dbSNP Id: rs368176448
ExAC: 10:105218074 G / A
gnomAD v2: 10-105218074-G-A
gnomAD v3: 10-103458317-G-A
gnomAD v4: 10-103458317-G-A
MyVariant Identifiers: chr10:g.105218074G>A (hg19) chr10:g.103458317G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103458317G>A , CM000672.2:g.103458317G>A GRCh38
NC_000010.10:g.105218074G>A , CM000672.1:g.105218074G>A GRCh37
NC_000010.9:g.105208064G>A NCBI36
NG_016855.1:g.5575C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000329905.6:c.435C>T MANE Select ENSP00000329926.6:p.Pro145=
ENST00000329905.5:c.435C>T ENSP00000329926.5:p.Pro145=
NM_001001412.3:c.435C>T NP_001001412.3:p.Pro145=
NM_001001412.4:c.435C>T MANE Select NP_001001412.3:p.Pro145=
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