Canonical Allele Identifier: CA2671575219

Gene: NFKB1

Linked Data

• gnomAD v4: 4-102501360-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102501360A>G , CM000666.2:g.102501360A>G	GRCh38
NC_000004.11:g.103422517A>G , CM000666.1:g.103422517A>G	GRCh37
NC_000004.10:g.103641549A>G	NCBI36
NG_050628.1:g.5032A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000507079.6:c.-482A>G	ENSP00000426147.2:n.-482A>G
ENST00000226574.9:c.-436A>G MANE Select	ENSP00000226574.4:n.-436A>G
ENST00000226574.8:c.-436A>G	ENSP00000226574.4:n.-436A>G
ENST00000394820.8:c.-436A>G	ENSP00000378297.4:n.-436A>G
NM_001165412.1:c.-436A>G	NP_001158884.1:n.-436A>G
NM_003998.3:c.-436A>G	NP_003989.2:n.-436A>G
XM_011532467.1:c.532T>C	XP_011530769.1:p.Ser178Pro
NR_136202.1:n.48+1079T>C
XM_024454067.1:c.-482A>G	XP_024309835.1:n.-482A>G
XM_024454069.1:c.-482A>G	XP_024309837.1:n.-482A>G
NM_003998.4:c.-436A>G MANE Select	NP_003989.2:n.-436A>G
NM_001165412.2:c.-436A>G	NP_001158884.1:n.-436A>G
NM_001382626.1:c.-506A>G	NP_001369555.1:n.-506A>G
NM_001382627.1:c.-506A>G	NP_001369556.1:n.-506A>G
NM_001382628.1:c.-429A>G	NP_001369557.1:n.-429A>G