Canonical Allele Identifier: CA28152893
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs771753130

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100540066T>A , CM000663.2:g.100540066T>A GRCh38
NC_000001.10:g.101005622T>A , CM000663.1:g.101005622T>A GRCh37
NC_000001.9:g.100778210T>A NCBI36
NG_053134.1:g.6895T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.1100T>A MANE Select ENSP00000314223.4:p.Val367Glu
ENST00000315033.4:c.1100T>A ENSP00000314223.4:p.Val367Glu
NM_022049.2:c.1100T>A NP_071332.2:p.Val367Glu
NM_022049.3:c.1100T>A MANE Select NP_071332.2:p.Val367Glu