Canonical Allele Identifier: CA1184191370
Gene: GPR88 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539997G= , CM000663.2:g.100539997G= GRCh38
NC_000001.10:g.101005553G= , CM000663.1:g.101005553G= GRCh37
NC_000001.9:g.100778141G= NCBI36
NG_053134.1:g.6826G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.1031G= MANE Select ENSP00000314223.4:p.Arg344=
ENST00000315033.4:c.1031G= ENSP00000314223.4:p.Arg344=
NM_022049.2:c.1031G= NP_071332.2:p.Arg344=
NM_022049.3:c.1031G= MANE Select NP_071332.2:p.Arg344=