Canonical Allele Identifier: CA469801522
Gene: ATOH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1970337
ClinVar RCV Id: RCV002730493
gnomAD v4: 10-68231654-G-A
MyVariant Identifiers: chr10:g.69991411G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231654G>A , CM000672.2:g.68231654G>A GRCh38
NC_000010.10:g.69991411G>A , CM000672.1:g.69991411G>A GRCh37
NC_000010.9:g.69661417G>A NCBI36
NG_031934.1:g.5460C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.24C>T MANE Select ENSP00000362777.3:p.Gly8=
ENST00000373673.4:c.24C>T ENSP00000362777.3:p.Gly8=
NM_145178.3:c.24C>T NP_660161.1:p.Gly8=
NM_145178.4:c.24C>T MANE Select NP_660161.1:p.Gly8=
Search 100 bp 5'
Search 100 bp 3'