Canonical Allele Identifier: CA376835883
Gene: ATOH7 HGNC NCBI

Linked Data

dbSNP Id: rs2044025947

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231427A>G , CM000672.2:g.68231427A>G GRCh38
NC_000010.10:g.69991184A>G , CM000672.1:g.69991184A>G GRCh37
NC_000010.9:g.69661190A>G NCBI36
NG_031934.1:g.5687T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.251T>C MANE Select ENSP00000362777.3:p.Met84Thr
ENST00000373673.4:c.251T>C ENSP00000362777.3:p.Met84Thr
NM_145178.3:c.251T>C NP_660161.1:p.Met84Thr
NM_145178.4:c.251T>C MANE Select NP_660161.1:p.Met84Thr