Canonical Allele Identifier: CA506108292
Gene: PIK3R2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2417964
ClinVar RCV Id: RCV003118073
dbSNP Id: rs2147944956
MyVariant Identifiers: chr19:g.18266827T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18156017T>G , CM000681.2:g.18156017T>G GRCh38
NC_000019.9:g.18266827T>G , CM000681.1:g.18266827T>G GRCh37
NC_000019.8:g.18127827T>G NCBI36
NG_033010.1:g.7840T>G
NG_033010.2:g.7840T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222254.13:c.138T>G MANE Select ENSP00000222254.6:p.Gly46=
ENST00000617130.5:c.138T>G ENSP00000477864.2:p.Gly46=
ENST00000617642.2:c.138T>G ENSP00000484714.2:p.Gly46=
ENST00000222254.12:c.138T>G ENSP00000222254.6:p.Gly46=
ENST00000426902.5:c.138T>G ENSP00000395636.1:p.Gly46=
ENST00000593731.1:c.138T>G ENSP00000471914.1:p.Gly46=
ENST00000617130.4:c.138T>G ENSP00000477864.1:p.Gly46=
ENST00000617642.1:c.138T>G ENSP00000484714.1:p.Gly46=
NM_005027.3:c.138T>G NP_005018.1:p.Gly46=
NR_073517.1:n.678T>G
NM_005027.4:c.138T>G MANE Select NP_005018.2:p.Gly46=
NR_073517.2:n.693T>G
NR_162071.1:n.693T>G