Canonical Allele Identifier: CA419317449
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs1261015106
gnomAD v3: 1-100539575-G-T
gnomAD v4: 1-100539575-G-T
MyVariant Identifiers: chr1:g.101005131G>T (hg19) chr1:g.100539575G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539575G>T , CM000663.2:g.100539575G>T GRCh38
NC_000001.10:g.101005131G>T , CM000663.1:g.101005131G>T GRCh37
NC_000001.9:g.100777719G>T NCBI36
NG_053134.1:g.6404G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.609G>T MANE Select ENSP00000314223.4:p.Ala203=
ENST00000315033.4:c.609G>T ENSP00000314223.4:p.Ala203=
NM_022049.2:c.609G>T NP_071332.2:p.Ala203=
NM_022049.3:c.609G>T MANE Select NP_071332.2:p.Ala203=
Search 100 bp 5'
Search 100 bp 3'