Canonical Allele Identifier: CA971113
Gene: GPR88 HGNC NCBI

Linked Data

ClinVar Variation Id: 1670374
ClinVar RCV Id: RCV002203665
dbSNP Id: rs756182133
ExAC: 1:101005218 C / T
gnomAD v2: 1-101005218-C-T
gnomAD v4: 1-100539662-C-T
MyVariant Identifiers: chr1:g.101005218C>T (hg19) chr1:g.100539662C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539662C>T , CM000663.2:g.100539662C>T GRCh38
NC_000001.10:g.101005218C>T , CM000663.1:g.101005218C>T GRCh37
NC_000001.9:g.100777806C>T NCBI36
NG_053134.1:g.6491C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.696C>T MANE Select ENSP00000314223.4:p.His232=
ENST00000315033.4:c.696C>T ENSP00000314223.4:p.His232=
NM_022049.2:c.696C>T NP_071332.2:p.His232=
NM_022049.3:c.696C>T MANE Select NP_071332.2:p.His232=
Search 100 bp 5'
Search 100 bp 3'