Canonical Allele Identifier: CA404800247
Gene: PIK3R2 HGNC NCBI

Linked Data

dbSNP Id: rs2147944963
gnomAD v4: 19-18156019-G-A
MyVariant Identifiers: chr19:g.18266829G>A (hg19) chr19:g.18156019G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18156019G>A , CM000681.2:g.18156019G>A GRCh38
NC_000019.9:g.18266829G>A , CM000681.1:g.18266829G>A GRCh37
NC_000019.8:g.18127829G>A NCBI36
NG_033010.1:g.7842G>A
NG_033010.2:g.7842G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222254.13:c.140G>A MANE Select ENSP00000222254.6:p.Gly47Asp
ENST00000617130.5:c.140G>A ENSP00000477864.2:p.Gly47Asp
ENST00000617642.2:c.140G>A ENSP00000484714.2:p.Gly47Asp
ENST00000222254.12:c.140G>A ENSP00000222254.6:p.Gly47Asp
ENST00000426902.5:c.140G>A ENSP00000395636.1:p.Gly47Asp
ENST00000593731.1:c.140G>A ENSP00000471914.1:p.Gly47Asp
ENST00000617130.4:c.140G>A ENSP00000477864.1:p.Gly47Asp
ENST00000617642.1:c.140G>A ENSP00000484714.1:p.Gly47Asp
NM_005027.3:c.140G>A NP_005018.1:p.Gly47Asp
NR_073517.1:n.680G>A
NM_005027.4:c.140G>A MANE Select NP_005018.2:p.Gly47Asp
NR_073517.2:n.695G>A
NR_162071.1:n.695G>A
Search 100 bp 5'
Search 100 bp 3'