Canonical Allele Identifier: CA971162
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs769337001
ExAC: 1:101005585 G / A
gnomAD v2: 1-101005585-G-A
gnomAD v4: 1-100540029-G-A
MyVariant Identifiers: chr1:g.101005585G>A (hg19) chr1:g.100540029G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100540029G>A , CM000663.2:g.100540029G>A GRCh38
NC_000001.10:g.101005585G>A , CM000663.1:g.101005585G>A GRCh37
NC_000001.9:g.100778173G>A NCBI36
NG_053134.1:g.6858G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.1063G>A MANE Select ENSP00000314223.4:p.Gly355Ser
ENST00000315033.4:c.1063G>A ENSP00000314223.4:p.Gly355Ser
NM_022049.2:c.1063G>A NP_071332.2:p.Gly355Ser
NM_022049.3:c.1063G>A MANE Select NP_071332.2:p.Gly355Ser
Search 100 bp 5'
Search 100 bp 3'