Canonical Allele Identifier: CA5674691
Gene: CALHM1 HGNC NCBI

Linked Data

dbSNP Id: rs138672499

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103458316C>T , CM000672.2:g.103458316C>T GRCh38
NC_000010.10:g.105218073C>T , CM000672.1:g.105218073C>T GRCh37
NC_000010.9:g.105208063C>T NCBI36
NG_016855.1:g.5576G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000329905.6:c.436G>A MANE Select ENSP00000329926.6:p.Gly146Ser
ENST00000329905.5:c.436G>A ENSP00000329926.5:p.Gly146Ser
NM_001001412.3:c.436G>A NP_001001412.3:p.Gly146Ser
NM_001001412.4:c.436G>A MANE Select NP_001001412.3:p.Gly146Ser