Canonical Allele Identifier: CA419188117
Gene: GPR88 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.101005482C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539926C>A , CM000663.2:g.100539926C>A GRCh38
NC_000001.10:g.101005482C>A , CM000663.1:g.101005482C>A GRCh37
NC_000001.9:g.100778070C>A NCBI36
NG_053134.1:g.6755C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.960C>A MANE Select ENSP00000314223.4:p.Ala320=
ENST00000315033.4:c.960C>A ENSP00000314223.4:p.Ala320=
NM_022049.2:c.960C>A NP_071332.2:p.Ala320=
NM_022049.3:c.960C>A MANE Select NP_071332.2:p.Ala320=