Canonical Allele Identifier: CA306164091
Gene: PIK3R2 HGNC NCBI

Linked Data

dbSNP Id: rs1054656723
gnomAD v4: 19-18156270-A-C
MyVariant Identifiers: chr19:g.18267080A>C (hg19) chr19:g.18156270A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18156270A>C , CM000681.2:g.18156270A>C GRCh38
NC_000019.9:g.18267080A>C , CM000681.1:g.18267080A>C GRCh37
NC_000019.8:g.18128080A>C NCBI36
NG_033010.1:g.8093A>C
NG_033010.2:g.8093A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000222254.13:c.322+69A>C MANE Select ENSP00000222254.6:n.322+69A>C
ENST00000617130.5:c.322+69A>C ENSP00000477864.2:n.322+69A>C
ENST00000617642.2:c.322+69A>C ENSP00000484714.2:n.322+69A>C
ENST00000222254.12:c.322+69A>C ENSP00000222254.6:n.322+69A>C
ENST00000426902.5:c.322+69A>C ENSP00000395636.1:n.322+69A>C
ENST00000593731.1:c.322+69A>C ENSP00000471914.1:n.322+69A>C
ENST00000617130.4:c.322+69A>C ENSP00000477864.1:n.322+69A>C
ENST00000617642.1:c.322+69A>C ENSP00000484714.1:n.322+69A>C
NM_005027.3:c.322+69A>C NP_005018.1:n.322+69A>C
NR_073517.1:n.862+69A>C
NM_005027.4:c.322+69A>C MANE Select NP_005018.2:n.322+69A>C
NR_073517.2:n.877+69A>C
NR_162071.1:n.877+69A>C
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