Canonical Allele Identifier: CA5523345
Gene: ATOH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1952068
ClinVar RCV Id: RCV002676708
dbSNP Id: rs763021073
ExAC: 10:69991129 G / A
gnomAD v2: 10-69991129-G-A
gnomAD v4: 10-68231372-G-A
MyVariant Identifiers: chr10:g.69991129G>A (hg19) chr10:g.68231372G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231372G>A , CM000672.2:g.68231372G>A GRCh38
NC_000010.10:g.69991129G>A , CM000672.1:g.69991129G>A GRCh37
NC_000010.9:g.69661135G>A NCBI36
NG_031934.1:g.5742C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.306C>T MANE Select ENSP00000362777.3:p.Phe102=
ENST00000373673.4:c.306C>T ENSP00000362777.3:p.Phe102=
NM_145178.3:c.306C>T NP_660161.1:p.Phe102=
NM_145178.4:c.306C>T MANE Select NP_660161.1:p.Phe102=
Search 100 bp 5'
Search 100 bp 3'