Canonical Allele Identifier: CA971143
Gene: GPR88 HGNC NCBI

Linked Data

ClinVar Variation Id: 1910126
ClinVar RCV Id: RCV002587663
dbSNP Id: rs776054029

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539955C>T , CM000663.2:g.100539955C>T GRCh38
NC_000001.10:g.101005511C>T , CM000663.1:g.101005511C>T GRCh37
NC_000001.9:g.100778099C>T NCBI36
NG_053134.1:g.6784C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.989C>T MANE Select ENSP00000314223.4:p.Ala330Val
ENST00000315033.4:c.989C>T ENSP00000314223.4:p.Ala330Val
NM_022049.2:c.989C>T NP_071332.2:p.Ala330Val
NM_022049.3:c.989C>T MANE Select NP_071332.2:p.Ala330Val