Canonical Allele Identifier: CA1917241528
Gene: ATOH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231435G= , CM000672.2:g.68231435G= GRCh38
NC_000010.10:g.69991192G= , CM000672.1:g.69991192G= GRCh37
NC_000010.9:g.69661198G= NCBI36
NG_031934.1:g.5679C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.243C= MANE Select ENSP00000362777.3:p.Thr81=
ENST00000373673.4:c.243C= ENSP00000362777.3:p.Thr81=
NM_145178.3:c.243C= NP_660161.1:p.Thr81=
NM_145178.4:c.243C= MANE Select NP_660161.1:p.Thr81=