Canonical Allele Identifier: CA1917241608
Gene: ATOH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231555C= , CM000672.2:g.68231555C= GRCh38
NC_000010.10:g.69991312C= , CM000672.1:g.69991312C= GRCh37
NC_000010.9:g.69661318C= NCBI36
NG_031934.1:g.5559G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.123G= MANE Select ENSP00000362777.3:p.Arg41=
ENST00000373673.4:c.123G= ENSP00000362777.3:p.Arg41=
NM_145178.3:c.123G= NP_660161.1:p.Arg41=
NM_145178.4:c.123G= MANE Select NP_660161.1:p.Arg41=