Canonical Allele Identifier: CA2671575305

Gene: NFKB1

Linked Data

• gnomAD v4: 4-102501455-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102501455G>T , CM000666.2:g.102501455G>T	GRCh38
NC_000004.11:g.103422612G>T , CM000666.1:g.103422612G>T	GRCh37
NC_000004.10:g.103641644G>T	NCBI36
NG_050628.1:g.5127G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507079.6:c.-387G>T	ENSP00000426147.2:n.-387G>T
ENST00000226574.9:c.-341G>T MANE Select	ENSP00000226574.4:n.-341G>T
ENST00000652619.1:c.-387G>T	ENSP00000499031.1:n.-387G>T
ENST00000226574.8:c.-341G>T	ENSP00000226574.4:n.-341G>T
ENST00000394820.8:c.-341G>T	ENSP00000378297.4:n.-341G>T
ENST00000511926.5:c.-387G>T	ENSP00000420904.1:n.-387G>T
NM_001165412.1:c.-341G>T	NP_001158884.1:n.-341G>T
NM_003998.3:c.-341G>T	NP_003989.2:n.-341G>T
XM_011532467.1:c.437C>A	XP_011530769.1:p.Pro146His
NR_136202.1:n.48+984C>A
XM_024454067.1:c.-387G>T	XP_024309835.1:n.-387G>T
XM_024454069.1:c.-387G>T	XP_024309837.1:n.-387G>T
NM_003998.4:c.-341G>T MANE Select	NP_003989.2:n.-341G>T
NM_001165412.2:c.-341G>T	NP_001158884.1:n.-341G>T
NM_001382626.1:c.-411G>T	NP_001369555.1:n.-411G>T
NM_001382627.1:c.-411G>T	NP_001369556.1:n.-411G>T
NM_001382628.1:c.-334G>T	NP_001369557.1:n.-334G>T