Canonical Allele Identifier: CA341393059
Gene: GPR88 HGNC NCBI

Linked Data

ClinVar Variation Id: 2544671
ClinVar RCV Id: RCV004320689
gnomAD v4: 1-100540035-G-A
MyVariant Identifiers: chr1:g.101005591G>A (hg19) chr1:g.100540035G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100540035G>A , CM000663.2:g.100540035G>A GRCh38
NC_000001.10:g.101005591G>A , CM000663.1:g.101005591G>A GRCh37
NC_000001.9:g.100778179G>A NCBI36
NG_053134.1:g.6864G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.1069G>A MANE Select ENSP00000314223.4:p.Ala357Thr
ENST00000315033.4:c.1069G>A ENSP00000314223.4:p.Ala357Thr
NM_022049.2:c.1069G>A NP_071332.2:p.Ala357Thr
NM_022049.3:c.1069G>A MANE Select NP_071332.2:p.Ala357Thr
Search 100 bp 5'
Search 100 bp 3'