Canonical Allele Identifier: CA208210092
Gene: ATOH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1949899
ClinVar RCV Id: RCV002659577
dbSNP Id: rs953948041

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231671A>G , CM000672.2:g.68231671A>G GRCh38
NC_000010.10:g.69991428A>G , CM000672.1:g.69991428A>G GRCh37
NC_000010.9:g.69661434A>G NCBI36
NG_031934.1:g.5443T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.7T>C MANE Select ENSP00000362777.3:p.Ser3Pro
ENST00000373673.4:c.7T>C ENSP00000362777.3:p.Ser3Pro
NM_145178.3:c.7T>C NP_660161.1:p.Ser3Pro
NM_145178.4:c.7T>C MANE Select NP_660161.1:p.Ser3Pro