Canonical Allele Identifier: CA341392760
Gene: GPR88 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539891T>A , CM000663.2:g.100539891T>A GRCh38
NC_000001.10:g.101005447T>A , CM000663.1:g.101005447T>A GRCh37
NC_000001.9:g.100778035T>A NCBI36
NG_053134.1:g.6720T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.925T>A MANE Select ENSP00000314223.4:p.Phe309Ile
ENST00000315033.4:c.925T>A ENSP00000314223.4:p.Phe309Ile
NM_022049.2:c.925T>A NP_071332.2:p.Phe309Ile
NM_022049.3:c.925T>A MANE Select NP_071332.2:p.Phe309Ile