Canonical Allele Identifier: CA341392077

Gene: GPR88

Linked Data

• dbSNP Id: rs1160022618
• gnomAD v2: 1-101005111-G-A
• gnomAD v4: 1-100539555-G-A
• MyVariant Identifiers: chr1:g.101005111G>A (hg19) ; chr1:g.100539555G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100539555G>A , CM000663.2:g.100539555G>A	GRCh38
NC_000001.10:g.101005111G>A , CM000663.1:g.101005111G>A	GRCh37
NC_000001.9:g.100777699G>A	NCBI36
NG_053134.1:g.6384G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315033.5:c.589G>A MANE Select	ENSP00000314223.4:p.Ala197Thr
ENST00000315033.4:c.589G>A	ENSP00000314223.4:p.Ala197Thr
NM_022049.2:c.589G>A	NP_071332.2:p.Ala197Thr
NM_022049.3:c.589G>A MANE Select	NP_071332.2:p.Ala197Thr