Canonical Allele Identifier: CA404814202

Gene: PIK3R2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000222254.13:c.1681A>C MANE Select	ENSP00000222254.6:p.Asn561His
ENST00000617130.5:c.*709A>C	ENSP00000477864.2:n.*709A>C
ENST00000617642.2:c.*709A>C	ENSP00000484714.2:n.*709A>C
ENST00000672815.1:c.531A>C	ENSP00000500792.1:n.531A>C
ENST00000674682.1:n.390A>C
ENST00000675271.1:n.742A>C
ENST00000222254.12:c.1681A>C	ENSP00000222254.6:p.Asn561His
ENST00000426902.5:c.*284A>C	ENSP00000395636.1:n.*284A>C
ENST00000464016.3:c.149A>C
ENST00000593731.1:c.1681A>C	ENSP00000471914.1:p.Asn561His
ENST00000617130.4:c.1681A>C	ENSP00000477864.1:p.Asn561His
NM_005027.3:c.1681A>C	NP_005018.1:p.Asn561His
NR_073517.1:n.2270A>C
NM_005027.4:c.1681A>C MANE Select	NP_005018.2:p.Asn561His
NR_073517.2:n.2285A>C
NR_162071.1:n.2019A>C