Canonical Allele Identifier: CA469801175
Gene: ATOH7 HGNC NCBI

Linked Data

dbSNP Id: rs2044027846
MyVariant Identifiers: chr10:g.69991335G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231578G>T , CM000672.2:g.68231578G>T GRCh38
NC_000010.10:g.69991335G>T , CM000672.1:g.69991335G>T GRCh37
NC_000010.9:g.69661341G>T NCBI36
NG_031934.1:g.5536C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.100C>A MANE Select ENSP00000362777.3:p.Arg34=
ENST00000373673.4:c.100C>A ENSP00000362777.3:p.Arg34=
NM_145178.3:c.100C>A NP_660161.1:p.Arg34=
NM_145178.4:c.100C>A MANE Select NP_660161.1:p.Arg34=