Canonical Allele Identifier: CA2610766182
Gene: CALHM1 HGNC NCBI

Linked Data

gnomAD v4: 10-103454033-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103454033C>A , CM000672.2:g.103454033C>A GRCh38
NC_000010.10:g.105213790C>A , CM000672.1:g.105213790C>A GRCh37
NC_000010.9:g.105203780C>A NCBI36
NG_016855.1:g.9859G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000329905.6:c.*1229G>T MANE Select ENSP00000329926.6:n.*1229G>T
ENST00000329905.5:c.*1229G>T ENSP00000329926.5:n.*1229G>T
NM_001001412.3:c.*1229G>T NP_001001412.3:n.*1229G>T
NM_001001412.4:c.*1229G>T MANE Select NP_001001412.3:n.*1229G>T
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