Canonical Allele Identifier: CA341392191
Gene: GPR88 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539613T>A , CM000663.2:g.100539613T>A GRCh38
NC_000001.10:g.101005169T>A , CM000663.1:g.101005169T>A GRCh37
NC_000001.9:g.100777757T>A NCBI36
NG_053134.1:g.6442T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.647T>A MANE Select ENSP00000314223.4:p.Val216Glu
ENST00000315033.4:c.647T>A ENSP00000314223.4:p.Val216Glu
NM_022049.2:c.647T>A NP_071332.2:p.Val216Glu
NM_022049.3:c.647T>A MANE Select NP_071332.2:p.Val216Glu