Canonical Allele Identifier: CA404814205

Gene: PIK3R2

Linked Data

• dbSNP Id: rs1057519801
• MyVariant Identifiers: chr19:g.18278061A>T (hg19) ; chr19:g.18167251A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18167251A>T , CM000681.2:g.18167251A>T	GRCh38
NC_000019.9:g.18278061A>T , CM000681.1:g.18278061A>T	GRCh37
NC_000019.8:g.18139061A>T	NCBI36
NG_033010.1:g.19074A>T
NG_033010.2:g.19074A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000222254.13:c.1681A>T MANE Select	ENSP00000222254.6:p.Asn561Tyr
ENST00000617130.5:c.*709A>T	ENSP00000477864.2:n.*709A>T
ENST00000617642.2:c.*709A>T	ENSP00000484714.2:n.*709A>T
ENST00000672815.1:c.531A>T	ENSP00000500792.1:n.531A>T
ENST00000674682.1:n.390A>T
ENST00000675271.1:n.742A>T
ENST00000222254.12:c.1681A>T	ENSP00000222254.6:p.Asn561Tyr
ENST00000426902.5:c.*284A>T	ENSP00000395636.1:n.*284A>T
ENST00000464016.3:c.149A>T
ENST00000593731.1:c.1681A>T	ENSP00000471914.1:p.Asn561Tyr
ENST00000617130.4:c.1681A>T	ENSP00000477864.1:p.Asn561Tyr
NM_005027.3:c.1681A>T	NP_005018.1:p.Asn561Tyr
NR_073517.1:n.2270A>T
NM_005027.4:c.1681A>T MANE Select	NP_005018.2:p.Asn561Tyr
NR_073517.2:n.2285A>T
NR_162071.1:n.2019A>T