Canonical Allele Identifier: CA341392425

Gene: GPR88

Linked Data

• dbSNP Id: rs1320888434
• gnomAD v3: 1-100539723-G-C
• gnomAD v4: 1-100539723-G-C
• MyVariant Identifiers: chr1:g.101005279G>C (hg19) ; chr1:g.100539723G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100539723G>C , CM000663.2:g.100539723G>C	GRCh38
NC_000001.10:g.101005279G>C , CM000663.1:g.101005279G>C	GRCh37
NC_000001.9:g.100777867G>C	NCBI36
NG_053134.1:g.6552G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315033.5:c.757G>C MANE Select	ENSP00000314223.4:p.Ala253Pro
ENST00000315033.4:c.757G>C	ENSP00000314223.4:p.Ala253Pro
NM_022049.2:c.757G>C	NP_071332.2:p.Ala253Pro
NM_022049.3:c.757G>C MANE Select	NP_071332.2:p.Ala253Pro