Canonical Allele Identifier: CA404800583
Gene: PIK3R2 HGNC NCBI

Linked Data

dbSNP Id: rs1191996614
MyVariant Identifiers: chr19:g.18266909T>G (hg19) chr19:g.18156099T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18156099T>G , CM000681.2:g.18156099T>G GRCh38
NC_000019.9:g.18266909T>G , CM000681.1:g.18266909T>G GRCh37
NC_000019.8:g.18127909T>G NCBI36
NG_033010.1:g.7922T>G
NG_033010.2:g.7922T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222254.13:c.220T>G MANE Select ENSP00000222254.6:p.Tyr74Asp
ENST00000617130.5:c.220T>G ENSP00000477864.2:p.Tyr74Asp
ENST00000617642.2:c.220T>G ENSP00000484714.2:p.Tyr74Asp
ENST00000222254.12:c.220T>G ENSP00000222254.6:p.Tyr74Asp
ENST00000426902.5:c.220T>G ENSP00000395636.1:p.Tyr74Asp
ENST00000593731.1:c.220T>G ENSP00000471914.1:p.Tyr74Asp
ENST00000617130.4:c.220T>G ENSP00000477864.1:p.Tyr74Asp
ENST00000617642.1:c.220T>G ENSP00000484714.1:p.Tyr74Asp
NM_005027.3:c.220T>G NP_005018.1:p.Tyr74Asp
NR_073517.1:n.760T>G
NM_005027.4:c.220T>G MANE Select NP_005018.2:p.Tyr74Asp
NR_073517.2:n.775T>G
NR_162071.1:n.775T>G
Search 100 bp 5'
Search 100 bp 3'