Canonical Allele Identifier: CA376837378
Gene: ATOH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2051478
ClinVar RCV Id: RCV002927281

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231569T>C , CM000672.2:g.68231569T>C GRCh38
NC_000010.10:g.69991326T>C , CM000672.1:g.69991326T>C GRCh37
NC_000010.9:g.69661332T>C NCBI36
NG_031934.1:g.5545A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.109A>G MANE Select ENSP00000362777.3:p.Ser37Gly
ENST00000373673.4:c.109A>G ENSP00000362777.3:p.Ser37Gly
NM_145178.3:c.109A>G NP_660161.1:p.Ser37Gly
NM_145178.4:c.109A>G MANE Select NP_660161.1:p.Ser37Gly