Canonical Allele Identifier: CA404800496
Gene: PIK3R2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1369322
ClinVar RCV Id: RCV001870568
dbSNP Id: rs2147945157
gnomAD v4: 19-18156078-C-T
MyVariant Identifiers: chr19:g.18266888C>T (hg19) chr19:g.18156078C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18156078C>T , CM000681.2:g.18156078C>T GRCh38
NC_000019.9:g.18266888C>T , CM000681.1:g.18266888C>T GRCh37
NC_000019.8:g.18127888C>T NCBI36
NG_033010.1:g.7901C>T
NG_033010.2:g.7901C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222254.13:c.199C>T MANE Select ENSP00000222254.6:p.Arg67Ter
ENST00000617130.5:c.199C>T ENSP00000477864.2:p.Arg67Ter
ENST00000617642.2:c.199C>T ENSP00000484714.2:p.Arg67Ter
ENST00000222254.12:c.199C>T ENSP00000222254.6:p.Arg67Ter
ENST00000426902.5:c.199C>T ENSP00000395636.1:p.Arg67Ter
ENST00000593731.1:c.199C>T ENSP00000471914.1:p.Arg67Ter
ENST00000617130.4:c.199C>T ENSP00000477864.1:p.Arg67Ter
ENST00000617642.1:c.199C>T ENSP00000484714.1:p.Arg67Ter
NM_005027.3:c.199C>T NP_005018.1:p.Arg67Ter
NR_073517.1:n.739C>T
NM_005027.4:c.199C>T MANE Select NP_005018.2:p.Arg67Ter
NR_073517.2:n.754C>T
NR_162071.1:n.754C>T
Search 100 bp 5'
Search 100 bp 3'