Canonical Allele Identifier: CA2735862673
Gene: PIK3R2 HGNC NCBI

Linked Data

dbSNP Id: rs2147945495

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18156214C>G , CM000681.2:g.18156214C>G GRCh38
NC_000019.9:g.18267024C>G , CM000681.1:g.18267024C>G GRCh37
NC_000019.8:g.18128024C>G NCBI36
NG_033010.1:g.8037C>G
NG_033010.2:g.8037C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222254.13:c.322+13C>G MANE Select ENSP00000222254.6:n.322+13C>G
ENST00000617130.5:c.322+13C>G ENSP00000477864.2:n.322+13C>G
ENST00000617642.2:c.322+13C>G ENSP00000484714.2:n.322+13C>G
ENST00000222254.12:c.322+13C>G ENSP00000222254.6:n.322+13C>G
ENST00000426902.5:c.322+13C>G ENSP00000395636.1:n.322+13C>G
ENST00000593731.1:c.322+13C>G ENSP00000471914.1:n.322+13C>G
ENST00000617130.4:c.322+13C>G ENSP00000477864.1:n.322+13C>G
ENST00000617642.1:c.322+13C>G ENSP00000484714.1:n.322+13C>G
NM_005027.3:c.322+13C>G NP_005018.1:n.322+13C>G
NR_073517.1:n.862+13C>G
NM_005027.4:c.322+13C>G MANE Select NP_005018.2:n.322+13C>G
NR_073517.2:n.877+13C>G
NR_162071.1:n.877+13C>G