Canonical Allele Identifier: CA341392226
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs2101527644
gnomAD v4: 1-100539631-G-T
MyVariant Identifiers: chr1:g.101005187G>T (hg19) chr1:g.100539631G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539631G>T , CM000663.2:g.100539631G>T GRCh38
NC_000001.10:g.101005187G>T , CM000663.1:g.101005187G>T GRCh37
NC_000001.9:g.100777775G>T NCBI36
NG_053134.1:g.6460G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.665G>T MANE Select ENSP00000314223.4:p.Ser222Ile
ENST00000315033.4:c.665G>T ENSP00000314223.4:p.Ser222Ile
NM_022049.2:c.665G>T NP_071332.2:p.Ser222Ile
NM_022049.3:c.665G>T MANE Select NP_071332.2:p.Ser222Ile
Search 100 bp 5'
Search 100 bp 3'