Canonical Allele Identifier: CA377895696

Gene: NFKB2

Linked Data

• ClinVar Variation Id: 2982582
• ClinVar RCV Id: RCV003845213
• MyVariant Identifiers: chr10:g.104155729T>G (hg19) ; chr10:g.102395972T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102395972T>G , CM000672.2:g.102395972T>G	GRCh38
NC_000010.10:g.104155729T>G , CM000672.1:g.104155729T>G	GRCh37
NC_000010.9:g.104145719T>G	NCBI36
NG_033874.1:g.6863T>G
NG_033874.2:g.6863T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697881.1:n.11T>G
ENST00000189444.11:c.13T>G	ENSP00000189444.6:p.Tyr5Asp
ENST00000369966.8:c.13T>G	ENSP00000358983.3:p.Tyr5Asp
ENST00000428099.6:c.13T>G	ENSP00000410256.1:p.Tyr5Asp
ENST00000471698.6:n.266T>G
ENST00000652277.1:c.13T>G	ENSP00000498308.1:p.Tyr5Asp
ENST00000661543.1:c.13T>G MANE Select	ENSP00000499294.1:p.Tyr5Asp
ENST00000189444.10:c.13T>G	ENSP00000189444.6:p.Tyr5Asp
ENST00000369966.7:c.13T>G	ENSP00000358983.3:p.Tyr5Asp
ENST00000428099.5:c.13T>G	ENSP00000410256.1:p.Tyr5Asp
ENST00000467116.5:n.176T>G
ENST00000471698.5:c.13T>G	ENSP00000471586.1:p.Tyr5Asp
ENST00000601386.5:c.13T>G	ENSP00000470826.1:p.Tyr5Asp
ENST00000610498.1:c.13T>G	ENSP00000480211.1:p.Tyr5Asp
NM_001077494.3:c.13T>G	NP_001070962.1:p.Tyr5Asp
NM_001261403.2:c.13T>G	NP_001248332.1:p.Tyr5Asp
NM_001288724.1:c.13T>G	NP_001275653.1:p.Tyr5Asp
NM_002502.5:c.13T>G	NP_002493.3:p.Tyr5Asp
XM_005269860.1:c.13T>G	XP_005269917.1:p.Tyr5Asp
XM_005269861.3:c.13T>G	XP_005269918.1:p.Tyr5Asp
NM_001322934.1:c.13T>G	NP_001309863.1:p.Tyr5Asp
NM_001322935.1:c.13T>G	NP_001309864.1:p.Tyr5Asp
XM_017016278.1:c.540T>G	XP_016871767.1:p.Ala180=
XM_024448026.1:c.-349T>G	XP_024303794.1:n.-349T>G
XM_024448027.1:c.-1268T>G	XP_024303795.1:n.-1268T>G
NM_001261403.3:c.13T>G	NP_001248332.1:p.Tyr5Asp
NM_001322934.2:c.13T>G MANE Select	NP_001309863.1:p.Tyr5Asp
NM_002502.6:c.13T>G	NP_002493.3:p.Tyr5Asp