Canonical Allele Identifier: CA1405314224

Gene: PIK3CB

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138759702G>T , CM000665.2:g.138759702G>T	GRCh38
NC_000003.11:g.138478544G>T , CM000665.1:g.138478544G>T	GRCh37
NC_000003.10:g.139961234G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674063.1:c.-16-343C>A MANE Select	ENSP00000501150.1:n.-16-343C>A
ENST00000461451.1:c.-16-343C>A	ENSP00000420399.1:n.-16-343C>A
ENST00000462898.5:c.-16-343C>A	ENSP00000420108.1:n.-16-343C>A
ENST00000465581.1:c.-16-343C>A	ENSP00000417329.1:n.-16-343C>A
ENST00000477593.5:c.-16-343C>A	ENSP00000418143.1:n.-16-343C>A
ENST00000483968.5:c.-16-343C>A	ENSP00000419857.1:n.-16-343C>A
XM_005247530.2:c.-16-343C>A	XP_005247587.1:n.-16-343C>A
XM_006713659.2:c.-16-343C>A	XP_006713722.1:n.-16-343C>A
XM_011512895.1:c.-16-343C>A	XP_011511197.1:n.-16-343C>A
XM_006713659.3:c.-16-343C>A	XP_006713722.1:n.-16-343C>A
XM_011512895.2:c.-16-343C>A	XP_011511197.1:n.-16-343C>A
XM_017006619.1:c.-16-343C>A	XP_016862108.1:n.-16-343C>A
NM_006219.3:c.-16-343C>A MANE Select	NP_006210.1:n.-16-343C>A