Canonical Allele Identifier: CA341392213
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs1236400482

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539625G>A , CM000663.2:g.100539625G>A GRCh38
NC_000001.10:g.101005181G>A , CM000663.1:g.101005181G>A GRCh37
NC_000001.9:g.100777769G>A NCBI36
NG_053134.1:g.6454G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.659G>A MANE Select ENSP00000314223.4:p.Arg220His
ENST00000315033.4:c.659G>A ENSP00000314223.4:p.Arg220His
NM_022049.2:c.659G>A NP_071332.2:p.Arg220His
NM_022049.3:c.659G>A MANE Select NP_071332.2:p.Arg220His