Canonical Allele Identifier: CA1917241568
Gene: ATOH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231504A= , CM000672.2:g.68231504A= GRCh38
NC_000010.10:g.69991261A= , CM000672.1:g.69991261A= GRCh37
NC_000010.9:g.69661267A= NCBI36
NG_031934.1:g.5610T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.174T= MANE Select ENSP00000362777.3:p.Thr58=
ENST00000373673.4:c.174T= ENSP00000362777.3:p.Thr58=
NM_145178.3:c.174T= NP_660161.1:p.Thr58=
NM_145178.4:c.174T= MANE Select NP_660161.1:p.Thr58=