Canonical Allele Identifier: CA376835435
Gene: ATOH7 HGNC NCBI

Linked Data

dbSNP Id: rs1397317385
gnomAD v2: 10-69991082-C-T
gnomAD v3: 10-68231325-C-T
gnomAD v4: 10-68231325-C-T
MyVariant Identifiers: chr10:g.69991082C>T (hg19) chr10:g.68231325C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231325C>T , CM000672.2:g.68231325C>T GRCh38
NC_000010.10:g.69991082C>T , CM000672.1:g.69991082C>T GRCh37
NC_000010.9:g.69661088C>T NCBI36
NG_031934.1:g.5789G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.353G>A MANE Select ENSP00000362777.3:p.Arg118His
ENST00000373673.4:c.353G>A ENSP00000362777.3:p.Arg118His
NM_145178.3:c.353G>A NP_660161.1:p.Arg118His
NM_145178.4:c.353G>A MANE Select NP_660161.1:p.Arg118His
Search 100 bp 5'
Search 100 bp 3'