Canonical Allele Identifier: CA404807946

Gene: PIK3R2

Linked Data

• dbSNP Id: rs587776934
• MyVariant Identifiers: chr19:g.18273784G>C (hg19) ; chr19:g.18162974G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18162974G>C , CM000681.2:g.18162974G>C	GRCh38
NC_000019.9:g.18273784G>C , CM000681.1:g.18273784G>C	GRCh37
NC_000019.8:g.18134784G>C	NCBI36
NG_033010.1:g.14797G>C
NG_033010.2:g.14797G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222254.13:c.1117G>C MANE Select	ENSP00000222254.6:p.Gly373Arg
ENST00000617130.5:c.*96G>C	ENSP00000477864.2:n.*96G>C
ENST00000617642.2:c.*96G>C	ENSP00000484714.2:n.*96G>C
ENST00000675271.1:n.63G>C
ENST00000222254.12:c.1117G>C	ENSP00000222254.6:p.Gly373Arg
ENST00000426902.5:c.1117G>C	ENSP00000395636.1:p.Gly373Arg
ENST00000593731.1:c.1117G>C	ENSP00000471914.1:p.Gly373Arg
ENST00000617130.4:c.1117G>C	ENSP00000477864.1:p.Gly373Arg
ENST00000617642.1:c.1117G>C	ENSP00000484714.1:p.Gly373Arg
NM_005027.3:c.1117G>C	NP_005018.1:p.Gly373Arg
NR_073517.1:n.1657G>C
NM_005027.4:c.1117G>C MANE Select	NP_005018.2:p.Gly373Arg
NR_073517.2:n.1672G>C
NR_162071.1:n.1455G>C