Canonical Allele Identifier: CA1184190825
Gene: GPR88 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539558G= , CM000663.2:g.100539558G= GRCh38
NC_000001.10:g.101005114G= , CM000663.1:g.101005114G= GRCh37
NC_000001.9:g.100777702G= NCBI36
NG_053134.1:g.6387G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.592G= MANE Select ENSP00000314223.4:p.Ala198=
ENST00000315033.4:c.592G= ENSP00000314223.4:p.Ala198=
NM_022049.2:c.592G= NP_071332.2:p.Ala198=
NM_022049.3:c.592G= MANE Select NP_071332.2:p.Ala198=
Search 100 bp 5'
Search 100 bp 3'