Canonical Allele Identifier: CA404800660
Gene: PIK3R2 HGNC NCBI

Linked Data

dbSNP Id: rs2147945240
gnomAD v4: 19-18156117-C-A
MyVariant Identifiers: chr19:g.18266927C>A (hg19) chr19:g.18156117C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18156117C>A , CM000681.2:g.18156117C>A GRCh38
NC_000019.9:g.18266927C>A , CM000681.1:g.18266927C>A GRCh37
NC_000019.8:g.18127927C>A NCBI36
NG_033010.1:g.7940C>A
NG_033010.2:g.7940C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222254.13:c.238C>A MANE Select ENSP00000222254.6:p.Pro80Thr
ENST00000617130.5:c.238C>A ENSP00000477864.2:p.Pro80Thr
ENST00000617642.2:c.238C>A ENSP00000484714.2:p.Pro80Thr
ENST00000222254.12:c.238C>A ENSP00000222254.6:p.Pro80Thr
ENST00000426902.5:c.238C>A ENSP00000395636.1:p.Pro80Thr
ENST00000593731.1:c.238C>A ENSP00000471914.1:p.Pro80Thr
ENST00000617130.4:c.238C>A ENSP00000477864.1:p.Pro80Thr
ENST00000617642.1:c.238C>A ENSP00000484714.1:p.Pro80Thr
NM_005027.3:c.238C>A NP_005018.1:p.Pro80Thr
NR_073517.1:n.778C>A
NM_005027.4:c.238C>A MANE Select NP_005018.2:p.Pro80Thr
NR_073517.2:n.793C>A
NR_162071.1:n.793C>A
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