Canonical Allele Identifier: CA28152852
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs868001483
gnomAD v4: 1-100539562-C-T
MyVariant Identifiers: chr1:g.101005118C>T (hg19) chr1:g.100539562C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539562C>T , CM000663.2:g.100539562C>T GRCh38
NC_000001.10:g.101005118C>T , CM000663.1:g.101005118C>T GRCh37
NC_000001.9:g.100777706C>T NCBI36
NG_053134.1:g.6391C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.596C>T MANE Select ENSP00000314223.4:p.Ala199Val
ENST00000315033.4:c.596C>T ENSP00000314223.4:p.Ala199Val
NM_022049.2:c.596C>T NP_071332.2:p.Ala199Val
NM_022049.3:c.596C>T MANE Select NP_071332.2:p.Ala199Val
Search 100 bp 5'
Search 100 bp 3'