Canonical Allele Identifier: CA341392973
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs1309477508
gnomAD v2: 1-101005547-A-G
gnomAD v4: 1-100539991-A-G
MyVariant Identifiers: chr1:g.101005547A>G (hg19) chr1:g.100539991A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539991A>G , CM000663.2:g.100539991A>G GRCh38
NC_000001.10:g.101005547A>G , CM000663.1:g.101005547A>G GRCh37
NC_000001.9:g.100778135A>G NCBI36
NG_053134.1:g.6820A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.1025A>G MANE Select ENSP00000314223.4:p.Glu342Gly
ENST00000315033.4:c.1025A>G ENSP00000314223.4:p.Glu342Gly
NM_022049.2:c.1025A>G NP_071332.2:p.Glu342Gly
NM_022049.3:c.1025A>G MANE Select NP_071332.2:p.Glu342Gly
Search 100 bp 5'
Search 100 bp 3'