Canonical Allele Identifier: CA376837976
Gene: ATOH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1352319
ClinVar RCV Id: RCV002047514
dbSNP Id: rs1426761957

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231656C>A , CM000672.2:g.68231656C>A GRCh38
NC_000010.10:g.69991413C>A , CM000672.1:g.69991413C>A GRCh37
NC_000010.9:g.69661419C>A NCBI36
NG_031934.1:g.5458G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.22G>T MANE Select ENSP00000362777.3:p.Gly8Cys
ENST00000373673.4:c.22G>T ENSP00000362777.3:p.Gly8Cys
NM_145178.3:c.22G>T NP_660161.1:p.Gly8Cys
NM_145178.4:c.22G>T MANE Select NP_660161.1:p.Gly8Cys