Canonical Allele Identifier: CA469801498
Gene: ATOH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1123723
ClinVar RCV Id: RCV001454866
dbSNP Id: rs1311245597
gnomAD v2: 10-69991408-C-A
gnomAD v3: 10-68231651-C-A
gnomAD v4: 10-68231651-C-A
MyVariant Identifiers: chr10:g.69991408C>A (hg19) chr10:g.68231651C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231651C>A , CM000672.2:g.68231651C>A GRCh38
NC_000010.10:g.69991408C>A , CM000672.1:g.69991408C>A GRCh37
NC_000010.9:g.69661414C>A NCBI36
NG_031934.1:g.5463G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.27G>T MANE Select ENSP00000362777.3:p.Pro9=
ENST00000373673.4:c.27G>T ENSP00000362777.3:p.Pro9=
NM_145178.3:c.27G>T NP_660161.1:p.Pro9=
NM_145178.4:c.27G>T MANE Select NP_660161.1:p.Pro9=
Search 100 bp 5'
Search 100 bp 3'