Canonical Allele Identifier: CA170630

Gene: ATOH7

Linked Data

• ClinVar Variation Id: 144067
• ClinVar RCV Id: RCV000133579
• dbSNP Id: rs587777666
• MyVariant Identifiers: chr10:g.69991299T>G (hg19) ; chr10:g.68231542T>G (hg38)
• PubMed: PMID:11527934 ; PMID:22645276

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68231542T>G , CM000672.2:g.68231542T>G	GRCh38
NC_000010.10:g.69991299T>G , CM000672.1:g.69991299T>G	GRCh37
NC_000010.9:g.69661305T>G	NCBI36
NG_031934.1:g.5572A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373673.5:c.136A>C MANE Select	ENSP00000362777.3:p.Asn46His
ENST00000373673.4:c.136A>C	ENSP00000362777.3:p.Asn46His
NM_145178.3:c.136A>C	NP_660161.1:p.Asn46His
NM_145178.4:c.136A>C MANE Select	NP_660161.1:p.Asn46His