Canonical Allele Identifier: CA378040461
Gene: CALHM1 HGNC NCBI

Linked Data

dbSNP Id: rs2033178097
gnomAD v4: 10-103458370-C-T
MyVariant Identifiers: chr10:g.105218127C>T (hg19) chr10:g.103458370C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103458370C>T , CM000672.2:g.103458370C>T GRCh38
NC_000010.10:g.105218127C>T , CM000672.1:g.105218127C>T GRCh37
NC_000010.9:g.105208117C>T NCBI36
NG_016855.1:g.5522G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000329905.6:c.382G>A MANE Select ENSP00000329926.6:p.Ala128Thr
ENST00000329905.5:c.382G>A ENSP00000329926.5:p.Ala128Thr
NM_001001412.3:c.382G>A NP_001001412.3:p.Ala128Thr
NM_001001412.4:c.382G>A MANE Select NP_001001412.3:p.Ala128Thr
Search 100 bp 5'
Search 100 bp 3'