Canonical Allele Identifier: CA376835442

Gene: ATOH7

Linked Data

• MyVariant Identifiers: chr10:g.69991085C>G (hg19) ; chr10:g.68231328C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68231328C>G , CM000672.2:g.68231328C>G	GRCh38
NC_000010.10:g.69991085C>G , CM000672.1:g.69991085C>G	GRCh37
NC_000010.9:g.69661091C>G	NCBI36
NG_031934.1:g.5786G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373673.5:c.350G>C MANE Select	ENSP00000362777.3:p.Gly117Ala
ENST00000373673.4:c.350G>C	ENSP00000362777.3:p.Gly117Ala
NM_145178.3:c.350G>C	NP_660161.1:p.Gly117Ala
NM_145178.4:c.350G>C MANE Select	NP_660161.1:p.Gly117Ala