Canonical Allele Identifier: CA1184190932
Gene: GPR88 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539653C= , CM000663.2:g.100539653C= GRCh38
NC_000001.10:g.101005209C= , CM000663.1:g.101005209C= GRCh37
NC_000001.9:g.100777797C= NCBI36
NG_053134.1:g.6482C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.687C= MANE Select ENSP00000314223.4:p.Leu229=
ENST00000315033.4:c.687C= ENSP00000314223.4:p.Leu229=
NM_022049.2:c.687C= NP_071332.2:p.Leu229=
NM_022049.3:c.687C= MANE Select NP_071332.2:p.Leu229=
Search 100 bp 5'
Search 100 bp 3'