Canonical Allele Identifier: CA419317584
Gene: GPR88 HGNC NCBI

Linked Data

gnomAD v4: 1-100539617-C-G
MyVariant Identifiers: chr1:g.101005173C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539617C>G , CM000663.2:g.100539617C>G GRCh38
NC_000001.10:g.101005173C>G , CM000663.1:g.101005173C>G GRCh37
NC_000001.9:g.100777761C>G NCBI36
NG_053134.1:g.6446C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.651C>G MANE Select ENSP00000314223.4:p.Arg217=
ENST00000315033.4:c.651C>G ENSP00000314223.4:p.Arg217=
NM_022049.2:c.651C>G NP_071332.2:p.Arg217=
NM_022049.3:c.651C>G MANE Select NP_071332.2:p.Arg217=
Search 100 bp 5'
Search 100 bp 3'