Canonical Allele Identifier: CA971150
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs760868833
ExAC: 1:101005543 G / C
gnomAD v2: 1-101005543-G-C
gnomAD v3: 1-100539987-G-C
gnomAD v4: 1-100539987-G-C
MyVariant Identifiers: chr1:g.101005543G>C (hg19) chr1:g.100539987G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539987G>C , CM000663.2:g.100539987G>C GRCh38
NC_000001.10:g.101005543G>C , CM000663.1:g.101005543G>C GRCh37
NC_000001.9:g.100778131G>C NCBI36
NG_053134.1:g.6816G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.1021G>C MANE Select ENSP00000314223.4:p.Glu341Gln
ENST00000315033.4:c.1021G>C ENSP00000314223.4:p.Glu341Gln
NM_022049.2:c.1021G>C NP_071332.2:p.Glu341Gln
NM_022049.3:c.1021G>C MANE Select NP_071332.2:p.Glu341Gln
Search 100 bp 5'
Search 100 bp 3'