Canonical Allele Identifier: CA341393094

Gene: GPR88

Linked Data

• dbSNP Id: rs1254135742
• gnomAD v2: 1-101005609-G-C
• gnomAD v4: 1-100540053-G-C
• MyVariant Identifiers: chr1:g.101005609G>C (hg19) ; chr1:g.100540053G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100540053G>C , CM000663.2:g.100540053G>C	GRCh38
NC_000001.10:g.101005609G>C , CM000663.1:g.101005609G>C	GRCh37
NC_000001.9:g.100778197G>C	NCBI36
NG_053134.1:g.6882G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315033.5:c.1087G>C MANE Select	ENSP00000314223.4:p.Ala363Pro
ENST00000315033.4:c.1087G>C	ENSP00000314223.4:p.Ala363Pro
NM_022049.2:c.1087G>C	NP_071332.2:p.Ala363Pro
NM_022049.3:c.1087G>C MANE Select	NP_071332.2:p.Ala363Pro