Canonical Allele Identifier: CA341392204
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs1651701719
gnomAD v3: 1-100539621-G-A
gnomAD v4: 1-100539621-G-A
MyVariant Identifiers: chr1:g.101005177G>A (hg19) chr1:g.100539621G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539621G>A , CM000663.2:g.100539621G>A GRCh38
NC_000001.10:g.101005177G>A , CM000663.1:g.101005177G>A GRCh37
NC_000001.9:g.100777765G>A NCBI36
NG_053134.1:g.6450G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.655G>A MANE Select ENSP00000314223.4:p.Val219Met
ENST00000315033.4:c.655G>A ENSP00000314223.4:p.Val219Met
NM_022049.2:c.655G>A NP_071332.2:p.Val219Met
NM_022049.3:c.655G>A MANE Select NP_071332.2:p.Val219Met
Search 100 bp 5'
Search 100 bp 3'