Canonical Allele Identifier: CA1184190880
Gene: GPR88 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539601A= , CM000663.2:g.100539601A= GRCh38
NC_000001.10:g.101005157A= , CM000663.1:g.101005157A= GRCh37
NC_000001.9:g.100777745A= NCBI36
NG_053134.1:g.6430A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.635A= MANE Select ENSP00000314223.4:p.Tyr212=
ENST00000315033.4:c.635A= ENSP00000314223.4:p.Tyr212=
NM_022049.2:c.635A= NP_071332.2:p.Tyr212=
NM_022049.3:c.635A= MANE Select NP_071332.2:p.Tyr212=
Search 100 bp 5'
Search 100 bp 3'