Canonical Allele Identifier: CA404800293
Gene: PIK3R2 HGNC NCBI

Linked Data

dbSNP Id: rs2147945003
gnomAD v4: 19-18156030-C-A
MyVariant Identifiers: chr19:g.18266840C>A (hg19) chr19:g.18156030C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18156030C>A , CM000681.2:g.18156030C>A GRCh38
NC_000019.9:g.18266840C>A , CM000681.1:g.18266840C>A GRCh37
NC_000019.8:g.18127840C>A NCBI36
NG_033010.1:g.7853C>A
NG_033010.2:g.7853C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222254.13:c.151C>A MANE Select ENSP00000222254.6:p.Pro51Thr
ENST00000617130.5:c.151C>A ENSP00000477864.2:p.Pro51Thr
ENST00000617642.2:c.151C>A ENSP00000484714.2:p.Pro51Thr
ENST00000222254.12:c.151C>A ENSP00000222254.6:p.Pro51Thr
ENST00000426902.5:c.151C>A ENSP00000395636.1:p.Pro51Thr
ENST00000593731.1:c.151C>A ENSP00000471914.1:p.Pro51Thr
ENST00000617130.4:c.151C>A ENSP00000477864.1:p.Pro51Thr
ENST00000617642.1:c.151C>A ENSP00000484714.1:p.Pro51Thr
NM_005027.3:c.151C>A NP_005018.1:p.Pro51Thr
NR_073517.1:n.691C>A
NM_005027.4:c.151C>A MANE Select NP_005018.2:p.Pro51Thr
NR_073517.2:n.706C>A
NR_162071.1:n.706C>A
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