Canonical Allele Identifier: CA469826886
Gene: ATOH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2001779
ClinVar RCV Id: RCV002815702
MyVariant Identifiers: chr10:g.69991144G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231387G>T , CM000672.2:g.68231387G>T GRCh38
NC_000010.10:g.69991144G>T , CM000672.1:g.69991144G>T GRCh37
NC_000010.9:g.69661150G>T NCBI36
NG_031934.1:g.5727C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.291C>A MANE Select ENSP00000362777.3:p.Ala97=
ENST00000373673.4:c.291C>A ENSP00000362777.3:p.Ala97=
NM_145178.3:c.291C>A NP_660161.1:p.Ala97=
NM_145178.4:c.291C>A MANE Select NP_660161.1:p.Ala97=
Search 100 bp 5'
Search 100 bp 3'