Canonical Allele Identifier: CA404800522
Gene: PIK3R2 HGNC NCBI

Linked Data

dbSNP Id: rs2147945175
gnomAD v4: 19-18156085-A-G
MyVariant Identifiers: chr19:g.18266895A>G (hg19) chr19:g.18156085A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18156085A>G , CM000681.2:g.18156085A>G GRCh38
NC_000019.9:g.18266895A>G , CM000681.1:g.18266895A>G GRCh37
NC_000019.8:g.18127895A>G NCBI36
NG_033010.1:g.7908A>G
NG_033010.2:g.7908A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222254.13:c.206A>G MANE Select ENSP00000222254.6:p.Asp69Gly
ENST00000617130.5:c.206A>G ENSP00000477864.2:p.Asp69Gly
ENST00000617642.2:c.206A>G ENSP00000484714.2:p.Asp69Gly
ENST00000222254.12:c.206A>G ENSP00000222254.6:p.Asp69Gly
ENST00000426902.5:c.206A>G ENSP00000395636.1:p.Asp69Gly
ENST00000593731.1:c.206A>G ENSP00000471914.1:p.Asp69Gly
ENST00000617130.4:c.206A>G ENSP00000477864.1:p.Asp69Gly
ENST00000617642.1:c.206A>G ENSP00000484714.1:p.Asp69Gly
NM_005027.3:c.206A>G NP_005018.1:p.Asp69Gly
NR_073517.1:n.746A>G
NM_005027.4:c.206A>G MANE Select NP_005018.2:p.Asp69Gly
NR_073517.2:n.761A>G
NR_162071.1:n.761A>G
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