Canonical Allele Identifier: CA341392150
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs867017297

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539594C>T , CM000663.2:g.100539594C>T GRCh38
NC_000001.10:g.101005150C>T , CM000663.1:g.101005150C>T GRCh37
NC_000001.9:g.100777738C>T NCBI36
NG_053134.1:g.6423C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.628C>T MANE Select ENSP00000314223.4:p.His210Tyr
ENST00000315033.4:c.628C>T ENSP00000314223.4:p.His210Tyr
NM_022049.2:c.628C>T NP_071332.2:p.His210Tyr
NM_022049.3:c.628C>T MANE Select NP_071332.2:p.His210Tyr