Canonical Allele Identifier: CA341392847
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs1188321053
gnomAD v2: 1-101005489-C-G
gnomAD v4: 1-100539933-C-G
MyVariant Identifiers: chr1:g.101005489C>G (hg19) chr1:g.100539933C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539933C>G , CM000663.2:g.100539933C>G GRCh38
NC_000001.10:g.101005489C>G , CM000663.1:g.101005489C>G GRCh37
NC_000001.9:g.100778077C>G NCBI36
NG_053134.1:g.6762C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.967C>G MANE Select ENSP00000314223.4:p.Leu323Val
ENST00000315033.4:c.967C>G ENSP00000314223.4:p.Leu323Val
NM_022049.2:c.967C>G NP_071332.2:p.Leu323Val
NM_022049.3:c.967C>G MANE Select NP_071332.2:p.Leu323Val
Search 100 bp 5'
Search 100 bp 3'