Canonical Allele Identifier: CA419317392
Gene: GPR88 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.101005113C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539557C>G , CM000663.2:g.100539557C>G GRCh38
NC_000001.10:g.101005113C>G , CM000663.1:g.101005113C>G GRCh37
NC_000001.9:g.100777701C>G NCBI36
NG_053134.1:g.6386C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.591C>G MANE Select ENSP00000314223.4:p.Ala197=
ENST00000315033.4:c.591C>G ENSP00000314223.4:p.Ala197=
NM_022049.2:c.591C>G NP_071332.2:p.Ala197=
NM_022049.3:c.591C>G MANE Select NP_071332.2:p.Ala197=
Search 100 bp 5'
Search 100 bp 3'