Canonical Allele Identifier: CA376837552
Gene: ATOH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1000291
ClinVar RCV Id: RCV001296404
dbSNP Id: rs2044028072
gnomAD v4: 10-68231595-G-C
MyVariant Identifiers: chr10:g.69991352G>C (hg19) chr10:g.68231595G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231595G>C , CM000672.2:g.68231595G>C GRCh38
NC_000010.10:g.69991352G>C , CM000672.1:g.69991352G>C GRCh37
NC_000010.9:g.69661358G>C NCBI36
NG_031934.1:g.5519C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.83C>G MANE Select ENSP00000362777.3:p.Thr28Arg
ENST00000373673.4:c.83C>G ENSP00000362777.3:p.Thr28Arg
NM_145178.3:c.83C>G NP_660161.1:p.Thr28Arg
NM_145178.4:c.83C>G MANE Select NP_660161.1:p.Thr28Arg
Search 100 bp 5'
Search 100 bp 3'