Canonical Allele Identifier: CA341392436
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs1651711855

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539729G>A , CM000663.2:g.100539729G>A GRCh38
NC_000001.10:g.101005285G>A , CM000663.1:g.101005285G>A GRCh37
NC_000001.9:g.100777873G>A NCBI36
NG_053134.1:g.6558G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.763G>A MANE Select ENSP00000314223.4:p.Gly255Ser
ENST00000315033.4:c.763G>A ENSP00000314223.4:p.Gly255Ser
NM_022049.2:c.763G>A NP_071332.2:p.Gly255Ser
NM_022049.3:c.763G>A MANE Select NP_071332.2:p.Gly255Ser