Canonical Allele Identifier: CA506108276
Gene: PIK3R2 HGNC NCBI

Linked Data

dbSNP Id: rs1249936035
gnomAD v3: 19-18156149-A-G
gnomAD v4: 19-18156149-A-G
MyVariant Identifiers: chr19:g.18266959A>G (hg19) chr19:g.18156149A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18156149A>G , CM000681.2:g.18156149A>G GRCh38
NC_000019.9:g.18266959A>G , CM000681.1:g.18266959A>G GRCh37
NC_000019.8:g.18127959A>G NCBI36
NG_033010.1:g.7972A>G
NG_033010.2:g.7972A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222254.13:c.270A>G MANE Select ENSP00000222254.6:p.Pro90=
ENST00000617130.5:c.270A>G ENSP00000477864.2:p.Pro90=
ENST00000617642.2:c.270A>G ENSP00000484714.2:p.Pro90=
ENST00000222254.12:c.270A>G ENSP00000222254.6:p.Pro90=
ENST00000426902.5:c.270A>G ENSP00000395636.1:p.Pro90=
ENST00000593731.1:c.270A>G ENSP00000471914.1:p.Pro90=
ENST00000617130.4:c.270A>G ENSP00000477864.1:p.Pro90=
ENST00000617642.1:c.270A>G ENSP00000484714.1:p.Pro90=
NM_005027.3:c.270A>G NP_005018.1:p.Pro90=
NR_073517.1:n.810A>G
NM_005027.4:c.270A>G MANE Select NP_005018.2:p.Pro90=
NR_073517.2:n.825A>G
NR_162071.1:n.825A>G
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