Canonical Allele Identifier: CA469801468
Gene: ATOH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.69991402C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231645C>A , CM000672.2:g.68231645C>A GRCh38
NC_000010.10:g.69991402C>A , CM000672.1:g.69991402C>A GRCh37
NC_000010.9:g.69661408C>A NCBI36
NG_031934.1:g.5469G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.33G>T MANE Select ENSP00000362777.3:p.Ala11=
ENST00000373673.4:c.33G>T ENSP00000362777.3:p.Ala11=
NM_145178.3:c.33G>T NP_660161.1:p.Ala11=
NM_145178.4:c.33G>T MANE Select NP_660161.1:p.Ala11=