Canonical Allele Identifier: CA341392168

Gene: GPR88

Linked Data

• dbSNP Id: rs1385106760
• gnomAD v3: 1-100539601-A-G
• gnomAD v4: 1-100539601-A-G
• MyVariant Identifiers: chr1:g.101005157A>G (hg19) ; chr1:g.100539601A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100539601A>G , CM000663.2:g.100539601A>G	GRCh38
NC_000001.10:g.101005157A>G , CM000663.1:g.101005157A>G	GRCh37
NC_000001.9:g.100777745A>G	NCBI36
NG_053134.1:g.6430A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315033.5:c.635A>G MANE Select	ENSP00000314223.4:p.Tyr212Cys
ENST00000315033.4:c.635A>G	ENSP00000314223.4:p.Tyr212Cys
NM_022049.2:c.635A>G	NP_071332.2:p.Tyr212Cys
NM_022049.3:c.635A>G MANE Select	NP_071332.2:p.Tyr212Cys