Canonical Allele Identifier: CA11757306

Gene: NFKB1

Linked Data

• ClinVar Variation Id: 1290273
• ClinVar RCV Id: RCV001716571
• dbSNP Id: rs230526
• gnomAD v2: 4-103458825-A-G
• gnomAD v3: 4-102537668-A-G
• gnomAD v4: 4-102537668-A-G
• MyVariant Identifiers: chr4:g.103458825A>G (hg19) ; chr4:g.102537668A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102537668A>G , CM000666.2:g.102537668A>G	GRCh38
NC_000004.11:g.103458825A>G , CM000666.1:g.103458825A>G	GRCh37
NG_050628.1:g.41340A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000507079.6:c.184-190A>G	ENSP00000426147.2:n.184-190A>G
ENST00000509165.2:c.160-190A>G	ENSP00000423877.2:n.160-190A>G
ENST00000697793.1:n.258-190A>G
ENST00000697794.1:c.118+7754A>G	ENSP00000513443.1:n.118+7754A>G
ENST00000697796.1:n.436-190A>G
ENST00000697797.1:n.354-190A>G
ENST00000697798.1:n.5612A>G
ENST00000226574.9:c.160-190A>G MANE Select	ENSP00000226574.4:n.160-190A>G
ENST00000652569.1:c.74-190A>G
ENST00000652619.1:c.181-190A>G	ENSP00000499031.1:n.181-190A>G
ENST00000226574.8:c.160-190A>G	ENSP00000226574.4:n.160-190A>G
ENST00000394820.8:c.157-190A>G	ENSP00000378297.4:n.157-190A>G
ENST00000502367.1:n.70A>G
ENST00000505458.5:c.157-190A>G	ENSP00000424790.1:n.157-190A>G
ENST00000507079.5:c.184-190A>G	ENSP00000426147.1:n.184-190A>G
ENST00000509165.1:c.160-190A>G	ENSP00000423877.1:n.160-190A>G
ENST00000511926.5:c.181-190A>G	ENSP00000420904.1:n.181-190A>G
ENST00000513803.5:n.42+40A>G
NM_001165412.1:c.157-190A>G	NP_001158884.1:n.157-190A>G
NM_003998.3:c.160-190A>G	NP_003989.2:n.160-190A>G
XM_011532006.1:c.181-190A>G	XP_011530308.1:n.181-190A>G
XM_011532007.1:c.157-190A>G	XP_011530309.1:n.157-190A>G
XM_011532008.1:c.160-190A>G	XP_011530310.1:n.160-190A>G
XM_011532009.1:c.-237-190A>G	XP_011530311.1:n.-237-190A>G
NM_001319226.1:c.157-190A>G	NP_001306155.1:n.157-190A>G
XM_011532006.2:c.181-190A>G	XP_011530308.1:n.181-190A>G
XM_024454067.1:c.184-190A>G	XP_024309835.1:n.184-190A>G
XM_024454068.1:c.160-190A>G	XP_024309836.1:n.160-190A>G
XM_024454069.1:c.184-190A>G	XP_024309837.1:n.184-190A>G
NM_003998.4:c.160-190A>G MANE Select	NP_003989.2:n.160-190A>G
NM_001165412.2:c.157-190A>G	NP_001158884.1:n.157-190A>G
NM_001319226.2:c.157-190A>G	NP_001306155.1:n.157-190A>G
NM_001382625.1:c.160-190A>G	NP_001369554.1:n.160-190A>G
NM_001382626.1:c.160-190A>G	NP_001369555.1:n.160-190A>G
NM_001382627.1:c.157-190A>G	NP_001369556.1:n.157-190A>G
NM_001382628.1:c.118-190A>G	NP_001369557.1:n.118-190A>G