Canonical Allele Identifier: CA1184190982
Gene: GPR88 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539680C= , CM000663.2:g.100539680C= GRCh38
NC_000001.10:g.101005236C= , CM000663.1:g.101005236C= GRCh37
NC_000001.9:g.100777824C= NCBI36
NG_053134.1:g.6509C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.714C= MANE Select ENSP00000314223.4:p.Pro238=
ENST00000315033.4:c.714C= ENSP00000314223.4:p.Pro238=
NM_022049.2:c.714C= NP_071332.2:p.Pro238=
NM_022049.3:c.714C= MANE Select NP_071332.2:p.Pro238=