Canonical Allele Identifier: CA404800539
Gene: PIK3R2 HGNC NCBI

Linked Data

gnomAD v4: 19-18156088-T-C
MyVariant Identifiers: chr19:g.18266898T>C (hg19) chr19:g.18156088T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18156088T>C , CM000681.2:g.18156088T>C GRCh38
NC_000019.9:g.18266898T>C , CM000681.1:g.18266898T>C GRCh37
NC_000019.8:g.18127898T>C NCBI36
NG_033010.1:g.7911T>C
NG_033010.2:g.7911T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000222254.13:c.209T>C MANE Select ENSP00000222254.6:p.Phe70Ser
ENST00000617130.5:c.209T>C ENSP00000477864.2:p.Phe70Ser
ENST00000617642.2:c.209T>C ENSP00000484714.2:p.Phe70Ser
ENST00000222254.12:c.209T>C ENSP00000222254.6:p.Phe70Ser
ENST00000426902.5:c.209T>C ENSP00000395636.1:p.Phe70Ser
ENST00000593731.1:c.209T>C ENSP00000471914.1:p.Phe70Ser
ENST00000617130.4:c.209T>C ENSP00000477864.1:p.Phe70Ser
ENST00000617642.1:c.209T>C ENSP00000484714.1:p.Phe70Ser
NM_005027.3:c.209T>C NP_005018.1:p.Phe70Ser
NR_073517.1:n.749T>C
NM_005027.4:c.209T>C MANE Select NP_005018.2:p.Phe70Ser
NR_073517.2:n.764T>C
NR_162071.1:n.764T>C
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