Canonical Allele Identifier: CA971141
Gene: GPR88 HGNC NCBI

Linked Data

ClinVar Variation Id: 1962330
ClinVar RCV Id: RCV002735074
dbSNP Id: rs746699331
ExAC: 1:101005480 G / A
gnomAD v2: 1-101005480-G-A
gnomAD v4: 1-100539924-G-A
MyVariant Identifiers: chr1:g.101005480G>A (hg19) chr1:g.100539924G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539924G>A , CM000663.2:g.100539924G>A GRCh38
NC_000001.10:g.101005480G>A , CM000663.1:g.101005480G>A GRCh37
NC_000001.9:g.100778068G>A NCBI36
NG_053134.1:g.6753G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.958G>A MANE Select ENSP00000314223.4:p.Ala320Thr
ENST00000315033.4:c.958G>A ENSP00000314223.4:p.Ala320Thr
NM_022049.2:c.958G>A NP_071332.2:p.Ala320Thr
NM_022049.3:c.958G>A MANE Select NP_071332.2:p.Ala320Thr
Search 100 bp 5'
Search 100 bp 3'