Canonical Allele Identifier: CA5664988

Gene: NFKB2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102401177C>T , CM000672.2:g.102401177C>T	GRCh38
NC_000010.10:g.104160934C>T , CM000672.1:g.104160934C>T	GRCh37
NC_000010.9:g.104150924C>T	NCBI36
NG_033874.1:g.12068C>T
NG_033874.2:g.12068C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001322934.2:c.2072-3C>T MANE Select	NP_001309863.1:n.2072-3C>T
ENST00000661543.1:c.2072-3C>T MANE Select	ENSP00000499294.1:n.2072-3C>T
NM_001077494.3:c.2072-3C>T	NP_001070962.1:n.2072-3C>T
NM_001261403.2:c.2072-3C>T	NP_001248332.1:n.2072-3C>T
NM_001261403.3:c.2072-3C>T	NP_001248332.1:n.2072-3C>T
NM_001288724.1:c.2072-3C>T	NP_001275653.1:n.2072-3C>T
NM_001322934.1:c.2072-3C>T	NP_001309863.1:n.2072-3C>T
NM_001322935.1:c.1946-3C>T	NP_001309864.1:n.1946-3C>T
NM_002502.5:c.2072-3C>T	NP_002493.3:n.2072-3C>T
NM_002502.6:c.2072-3C>T	NP_002493.3:n.2072-3C>T
ENST00000189444.10:c.2072-3C>T	ENSP00000189444.6:n.2072-3C>T
ENST00000189444.11:c.2072-3C>T	ENSP00000189444.6:n.2072-3C>T
ENST00000369966.7:c.2072-3C>T	ENSP00000358983.3:n.2072-3C>T
ENST00000369966.8:c.2072-3C>T	ENSP00000358983.3:n.2072-3C>T
ENST00000428099.5:c.2072-3C>T	ENSP00000410256.1:n.2072-3C>T
ENST00000428099.6:c.2072-3C>T	ENSP00000410256.1:n.2072-3C>T
ENST00000473400.1:n.478C>T
ENST00000651907.1:n.33-928C>T
ENST00000652277.1:c.2072-3C>T	ENSP00000498308.1:n.2072-3C>T
ENST00000697883.1:n.1022-3C>T
ENST00000697884.1:n.338-3C>T
ENST00000697920.1:n.307+686C>T
XM_005269860.1:c.2072-3C>T	XP_005269917.1:n.2072-3C>T
XM_005269861.3:c.2072-3C>T	XP_005269918.1:n.2072-3C>T
XM_011539830.1:c.1637-3C>T	XP_011538132.1:n.1637-3C>T
XM_011539830.3:c.1637-3C>T	XP_011538132.1:n.1637-3C>T
XM_011539831.1:c.1637-3C>T	XP_011538133.1:n.1637-3C>T
XM_011539831.2:c.1637-3C>T	XP_011538133.1:n.1637-3C>T
XM_017016278.1:c.2615-3C>T	XP_016871767.1:n.2615-3C>T
XM_024448026.1:c.1946-3C>T	XP_024303794.1:n.1946-3C>T
XM_024448027.1:c.1007-3C>T	XP_024303795.1:n.1007-3C>T