Canonical Allele Identifier: CA2838221481

Gene: PIK3C2B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.204451441C>T , CM000663.2:g.204451441C>T	GRCh38
NC_000001.10:g.204420569C>T , CM000663.1:g.204420569C>T	GRCh37
NC_000001.9:g.202687192C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683234.1:n.1482-1424G>A
ENST00000684373.1:c.2067-1424G>A MANE Select	ENSP00000507222.1:n.2067-1424G>A
ENST00000367187.7:c.2067-1424G>A	ENSP00000356155.3:n.2067-1424G>A
ENST00000424712.6:c.2067-1424G>A	ENSP00000400561.2:n.2067-1424G>A
NM_002646.3:c.2067-1424G>A	NP_002637.3:n.2067-1424G>A
XM_005245257.1:c.2067-1424G>A	XP_005245314.1:n.2067-1424G>A
XM_005245258.2:c.2067-1424G>A	XP_005245315.1:n.2067-1424G>A
XM_011509630.1:c.2067-1424G>A	XP_011507932.1:n.2067-1424G>A
XM_011509631.1:c.2067-1424G>A	XP_011507933.1:n.2067-1424G>A
XM_011509632.1:c.2067-1424G>A	XP_011507934.1:n.2067-1424G>A
XM_011509633.1:c.2067-1424G>A	XP_011507935.1:n.2067-1424G>A
XR_241085.1:n.2611-1424G>A
XR_241086.1:n.2611-1424G>A
XM_005245257.2:c.2067-1424G>A	XP_005245314.1:n.2067-1424G>A
XM_005245258.3:c.2067-1424G>A	XP_005245315.1:n.2067-1424G>A
XM_011509630.2:c.2067-1424G>A	XP_011507932.1:n.2067-1424G>A
XM_011509631.2:c.2067-1424G>A	XP_011507933.1:n.2067-1424G>A
XM_011509633.2:c.2067-1424G>A	XP_011507935.1:n.2067-1424G>A
XM_017001473.1:c.2067-1424G>A	XP_016856962.1:n.2067-1424G>A
XM_017001474.1:c.2067-1424G>A	XP_016856963.1:n.2067-1424G>A
XM_017001475.1:c.375-1424G>A	XP_016856964.1:n.375-1424G>A
XR_241085.2:n.2611-1424G>A
NM_001377334.1:c.2067-1424G>A MANE Select	NP_001364263.1:n.2067-1424G>A
NM_001377335.1:c.2067-1424G>A	NP_001364264.1:n.2067-1424G>A
NM_002646.4:c.2067-1424G>A	NP_002637.3:n.2067-1424G>A