Canonical Allele Identifier: CA2583525401
Gene: PIK3R2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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