Canonical Allele Identifier: CA208210036

Gene: ATOH7

Linked Data

• dbSNP Id: rs938026944
• MyVariant Identifiers: chr10:g.69991372G>C (hg19) ; chr10:g.68231615G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68231615G>C , CM000672.2:g.68231615G>C	GRCh38
NC_000010.10:g.69991372G>C , CM000672.1:g.69991372G>C	GRCh37
NC_000010.9:g.69661378G>C	NCBI36
NG_031934.1:g.5499C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373673.5:c.63C>G MANE Select	ENSP00000362777.3:p.Gly21=
ENST00000373673.4:c.63C>G	ENSP00000362777.3:p.Gly21=
NM_145178.3:c.63C>G	NP_660161.1:p.Gly21=
NM_145178.4:c.63C>G MANE Select	NP_660161.1:p.Gly21=