Canonical Allele Identifier: CA404801281
Gene: PIK3R2 HGNC NCBI

Linked Data

dbSNP Id: rs1444173990
MyVariant Identifiers: chr19:g.18267013T>G (hg19) chr19:g.18156203T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18156203T>G , CM000681.2:g.18156203T>G GRCh38
NC_000019.9:g.18267013T>G , CM000681.1:g.18267013T>G GRCh37
NC_000019.8:g.18128013T>G NCBI36
NG_033010.1:g.8026T>G
NG_033010.2:g.8026T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222254.13:c.322+2T>G MANE Select ENSP00000222254.6:n.322+2T>G
ENST00000617130.5:c.322+2T>G ENSP00000477864.2:n.322+2T>G
ENST00000617642.2:c.322+2T>G ENSP00000484714.2:n.322+2T>G
ENST00000222254.12:c.322+2T>G ENSP00000222254.6:n.322+2T>G
ENST00000426902.5:c.322+2T>G ENSP00000395636.1:n.322+2T>G
ENST00000593731.1:c.322+2T>G ENSP00000471914.1:n.322+2T>G
ENST00000617130.4:c.322+2T>G ENSP00000477864.1:n.322+2T>G
ENST00000617642.1:c.322+2T>G ENSP00000484714.1:n.322+2T>G
NM_005027.3:c.322+2T>G NP_005018.1:n.322+2T>G
NR_073517.1:n.862+2T>G
NM_005027.4:c.322+2T>G MANE Select NP_005018.2:n.322+2T>G
NR_073517.2:n.877+2T>G
NR_162071.1:n.877+2T>G
Search 100 bp 5'
Search 100 bp 3'