Canonical Allele Identifier: CA16618923
Gene: NFKB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 421588
ClinVar RCV Id: RCV000484648
dbSNP Id: rs1064795232

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102402282G>A , CM000672.2:g.102402282G>A GRCh38
NC_000010.10:g.104162039G>A , CM000672.1:g.104162039G>A GRCh37
NC_000010.9:g.104152029G>A NCBI36
NG_033874.1:g.13173G>A
NG_033874.2:g.13173G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000697883.1:n.1559G>A
ENST00000697920.1:n.308-54G>A
ENST00000189444.11:c.2606G>A ENSP00000189444.6:p.Ser869Asn
ENST00000369966.8:c.2609G>A ENSP00000358983.3:p.Ser870Asn
ENST00000428099.6:c.2606G>A ENSP00000410256.1:p.Ser869Asn
ENST00000651907.1:n.115G>A
ENST00000652277.1:c.2606G>A ENSP00000498308.1:p.Ser869Asn
ENST00000661543.1:c.2609G>A MANE Select ENSP00000499294.1:p.Ser870Asn
ENST00000189444.10:c.2606G>A ENSP00000189444.6:p.Ser869Asn
ENST00000369966.7:c.2609G>A ENSP00000358983.3:p.Ser870Asn
ENST00000428099.5:c.2606G>A ENSP00000410256.1:p.Ser869Asn
NM_001077494.3:c.2609G>A NP_001070962.1:p.Ser870Asn
NM_001261403.2:c.2606G>A NP_001248332.1:p.Ser869Asn
NM_001288724.1:c.2606G>A NP_001275653.1:p.Ser869Asn
NM_002502.5:c.2606G>A NP_002493.3:p.Ser869Asn
XM_005269860.1:c.2609G>A XP_005269917.1:p.Ser870Asn
XM_005269861.3:c.2609G>A XP_005269918.1:p.Ser870Asn
XM_011539830.1:c.2174G>A XP_011538132.1:p.Ser725Asn
XM_011539831.1:c.2174G>A XP_011538133.1:p.Ser725Asn
NM_001322934.1:c.2609G>A NP_001309863.1:p.Ser870Asn
NM_001322935.1:c.2483G>A NP_001309864.1:p.Ser828Asn
XM_011539830.3:c.2174G>A XP_011538132.1:p.Ser725Asn
XM_011539831.2:c.2174G>A XP_011538133.1:p.Ser725Asn
XM_017016278.1:c.3152G>A XP_016871767.1:p.Ser1051Asn
XM_024448026.1:c.2483G>A XP_024303794.1:p.Ser828Asn
XM_024448027.1:c.1544G>A XP_024303795.1:p.Ser515Asn
NM_001261403.3:c.2606G>A NP_001248332.1:p.Ser869Asn
NM_001322934.2:c.2609G>A MANE Select NP_001309863.1:p.Ser870Asn
NM_002502.6:c.2606G>A NP_002493.3:p.Ser869Asn