Canonical Allele Identifier: CA419188164
Gene: GPR88 HGNC NCBI

Linked Data

ClinVar Variation Id: 1529156
ClinVar RCV Id: RCV002096945
dbSNP Id: rs2101528468
gnomAD v4: 1-100539983-G-A
MyVariant Identifiers: chr1:g.101005539G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539983G>A , CM000663.2:g.100539983G>A GRCh38
NC_000001.10:g.101005539G>A , CM000663.1:g.101005539G>A GRCh37
NC_000001.9:g.100778127G>A NCBI36
NG_053134.1:g.6812G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.1017G>A MANE Select ENSP00000314223.4:p.Arg339=
ENST00000315033.4:c.1017G>A ENSP00000314223.4:p.Arg339=
NM_022049.2:c.1017G>A NP_071332.2:p.Arg339=
NM_022049.3:c.1017G>A MANE Select NP_071332.2:p.Arg339=
Search 100 bp 5'
Search 100 bp 3'