Canonical Allele Identifier: CA784580357

Gene: NFKB1

Linked Data

• dbSNP Id: rs1399392367
• gnomAD v3: 4-102501430-C-G
• gnomAD v4: 4-102501430-C-G
• MyVariant Identifiers: chr4:g.103422587C>G (hg19) ; chr4:g.102501430C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102501430C>G , CM000666.2:g.102501430C>G	GRCh38
NC_000004.11:g.103422587C>G , CM000666.1:g.103422587C>G	GRCh37
NC_000004.10:g.103641619C>G	NCBI36
NG_050628.1:g.5102C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507079.6:c.-412C>G	ENSP00000426147.2:n.-412C>G
ENST00000226574.9:c.-366C>G MANE Select	ENSP00000226574.4:n.-366C>G
ENST00000652619.1:c.-412C>G	ENSP00000499031.1:n.-412C>G
ENST00000226574.8:c.-366C>G	ENSP00000226574.4:n.-366C>G
ENST00000394820.8:c.-366C>G	ENSP00000378297.4:n.-366C>G
NM_001165412.1:c.-366C>G	NP_001158884.1:n.-366C>G
NM_003998.3:c.-366C>G	NP_003989.2:n.-366C>G
XM_011532467.1:c.462G>C	XP_011530769.1:p.Lys154Asn
NR_136202.1:n.48+1009G>C
XM_024454067.1:c.-412C>G	XP_024309835.1:n.-412C>G
XM_024454069.1:c.-412C>G	XP_024309837.1:n.-412C>G
NM_003998.4:c.-366C>G MANE Select	NP_003989.2:n.-366C>G
NM_001165412.2:c.-366C>G	NP_001158884.1:n.-366C>G
NM_001382626.1:c.-436C>G	NP_001369555.1:n.-436C>G
NM_001382627.1:c.-436C>G	NP_001369556.1:n.-436C>G
NM_001382628.1:c.-359C>G	NP_001369557.1:n.-359C>G