Canonical Allele Identifier: CA10698621

Gene: PIK3C2B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.204488208G>A , CM000663.2:g.204488208G>A	GRCh38
NC_000001.10:g.204457336G>A , CM000663.1:g.204457336G>A	GRCh37
NC_000001.9:g.202723959G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001377334.1:c.-85+6148C>T MANE Select	NP_001364263.1:n.-85+6148C>T
ENST00000684373.1:c.-85+6148C>T MANE Select	ENSP00000507222.1:n.-85+6148C>T
NM_001377335.1:c.-85+1608C>T	NP_001364264.1:n.-85+1608C>T
NM_002646.3:c.-85+1608C>T	NP_002637.3:n.-85+1608C>T
NM_002646.4:c.-85+1608C>T	NP_002637.3:n.-85+1608C>T
ENST00000367187.7:c.-85+1608C>T	ENSP00000356155.3:n.-85+1608C>T
ENST00000415899.1:c.-85+6148C>T	ENSP00000401795.1:n.-85+6148C>T
ENST00000415899.2:c.-85+1608C>T	ENSP00000401795.2:n.-85+1608C>T
ENST00000424712.6:c.-85+1608C>T	ENSP00000400561.2:n.-85+1608C>T
ENST00000429009.1:c.-85+1608C>T	ENSP00000409554.1:n.-85+1608C>T
XM_005245257.1:c.-85+6148C>T	XP_005245314.1:n.-85+6148C>T
XM_005245257.2:c.-85+6148C>T	XP_005245314.1:n.-85+6148C>T
XM_005245258.2:c.-85+6148C>T	XP_005245315.1:n.-85+6148C>T
XM_005245258.3:c.-85+6148C>T	XP_005245315.1:n.-85+6148C>T
XM_011509630.1:c.-85+1608C>T	XP_011507932.1:n.-85+1608C>T
XM_011509630.2:c.-85+1608C>T	XP_011507932.1:n.-85+1608C>T
XM_011509631.1:c.-85+1608C>T	XP_011507933.1:n.-85+1608C>T
XM_011509631.2:c.-85+1608C>T	XP_011507933.1:n.-85+1608C>T
XM_011509633.1:c.-85+6148C>T	XP_011507935.1:n.-85+6148C>T
XM_011509633.2:c.-85+6148C>T	XP_011507935.1:n.-85+6148C>T
XM_017001473.1:c.-85+1608C>T	XP_016856962.1:n.-85+1608C>T
XM_017001474.1:c.-223+6148C>T	XP_016856963.1:n.-223+6148C>T
XR_241085.1:n.460+6148C>T
XR_241085.2:n.460+6148C>T
XR_241086.1:n.460+6148C>T