Canonical Allele Identifier: CA506108302
Gene: PIK3R2 HGNC NCBI

Linked Data

dbSNP Id: rs1317987064
gnomAD v2: 19-18266830-C-T
gnomAD v3: 19-18156020-C-T
gnomAD v4: 19-18156020-C-T
COSMIC: COSM5364947
MyVariant Identifiers: chr19:g.18266830C>T (hg19) chr19:g.18156020C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18156020C>T , CM000681.2:g.18156020C>T GRCh38
NC_000019.9:g.18266830C>T , CM000681.1:g.18266830C>T GRCh37
NC_000019.8:g.18127830C>T NCBI36
NG_033010.1:g.7843C>T
NG_033010.2:g.7843C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222254.13:c.141C>T MANE Select ENSP00000222254.6:p.Gly47=
ENST00000617130.5:c.141C>T ENSP00000477864.2:p.Gly47=
ENST00000617642.2:c.141C>T ENSP00000484714.2:p.Gly47=
ENST00000222254.12:c.141C>T ENSP00000222254.6:p.Gly47=
ENST00000426902.5:c.141C>T ENSP00000395636.1:p.Gly47=
ENST00000593731.1:c.141C>T ENSP00000471914.1:p.Gly47=
ENST00000617130.4:c.141C>T ENSP00000477864.1:p.Gly47=
ENST00000617642.1:c.141C>T ENSP00000484714.1:p.Gly47=
NM_005027.3:c.141C>T NP_005018.1:p.Gly47=
NR_073517.1:n.681C>T
NM_005027.4:c.141C>T MANE Select NP_005018.2:p.Gly47=
NR_073517.2:n.696C>T
NR_162071.1:n.696C>T
Search 100 bp 5'
Search 100 bp 3'