Canonical Allele Identifier: CA404800930
Gene: PIK3R2 HGNC NCBI

Linked Data

gnomAD v4: 19-18156151-G-T
COSMIC: COSM6366011
MyVariant Identifiers: chr19:g.18266961G>T (hg19) chr19:g.18156151G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18156151G>T , CM000681.2:g.18156151G>T GRCh38
NC_000019.9:g.18266961G>T , CM000681.1:g.18266961G>T GRCh37
NC_000019.8:g.18127961G>T NCBI36
NG_033010.1:g.7974G>T
NG_033010.2:g.7974G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222254.13:c.272G>T MANE Select ENSP00000222254.6:p.Arg91Leu
ENST00000617130.5:c.272G>T ENSP00000477864.2:p.Arg91Leu
ENST00000617642.2:c.272G>T ENSP00000484714.2:p.Arg91Leu
ENST00000222254.12:c.272G>T ENSP00000222254.6:p.Arg91Leu
ENST00000426902.5:c.272G>T ENSP00000395636.1:p.Arg91Leu
ENST00000593731.1:c.272G>T ENSP00000471914.1:p.Arg91Leu
ENST00000617130.4:c.272G>T ENSP00000477864.1:p.Arg91Leu
ENST00000617642.1:c.272G>T ENSP00000484714.1:p.Arg91Leu
NM_005027.3:c.272G>T NP_005018.1:p.Arg91Leu
NR_073517.1:n.812G>T
NM_005027.4:c.272G>T MANE Select NP_005018.2:p.Arg91Leu
NR_073517.2:n.827G>T
NR_162071.1:n.827G>T
Search 100 bp 5'
Search 100 bp 3'