Canonical Allele Identifier: CA419317395
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs1651712642
gnomAD v3: 1-100539752-G-C
gnomAD v4: 1-100539752-G-C
MyVariant Identifiers: chr1:g.101005308G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539752G>C , CM000663.2:g.100539752G>C GRCh38
NC_000001.10:g.101005308G>C , CM000663.1:g.101005308G>C GRCh37
NC_000001.9:g.100777896G>C NCBI36
NG_053134.1:g.6581G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000315033.5:c.786G>C MANE Select ENSP00000314223.4:p.Pro262=
ENST00000315033.4:c.786G>C ENSP00000314223.4:p.Pro262=
NM_022049.2:c.786G>C NP_071332.2:p.Pro262=
NM_022049.3:c.786G>C MANE Select NP_071332.2:p.Pro262=
Search 100 bp 5'
Search 100 bp 3'