Canonical Allele Identifier: CA1917241667
Gene: ATOH7 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.7T= MANE Select ENSP00000362777.3:p.Ser3=
ENST00000373673.4:c.7T= ENSP00000362777.3:p.Ser3=
NM_145178.3:c.7T= NP_660161.1:p.Ser3=
NM_145178.4:c.7T= MANE Select NP_660161.1:p.Ser3=