Canonical Allele Identifier: CA971166
Gene: GPR88 HGNC NCBI

Linked Data

ClinVar Variation Id: 1991366
ClinVar RCV Id: RCV002771591
dbSNP Id: rs773946491
ExAC: 1:101005606 G / A
gnomAD v2: 1-101005606-G-A
gnomAD v3: 1-100540050-G-A
gnomAD v4: 1-100540050-G-A
MyVariant Identifiers: chr1:g.101005606G>A (hg19) chr1:g.100540050G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100540050G>A , CM000663.2:g.100540050G>A GRCh38
NC_000001.10:g.101005606G>A , CM000663.1:g.101005606G>A GRCh37
NC_000001.9:g.100778194G>A NCBI36
NG_053134.1:g.6879G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.1084G>A MANE Select ENSP00000314223.4:p.Val362Ile
ENST00000315033.4:c.1084G>A ENSP00000314223.4:p.Val362Ile
NM_022049.2:c.1084G>A NP_071332.2:p.Val362Ile
NM_022049.3:c.1084G>A MANE Select NP_071332.2:p.Val362Ile
Search 100 bp 5'
Search 100 bp 3'