Canonical Allele Identifier: CA1066141098
Gene: NFKB1 HGNC NCBI

Linked Data

dbSNP Id: rs1738998999
gnomAD v3: 4-102501355-G-A
gnomAD v4: 4-102501355-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501355G>A , CM000666.2:g.102501355G>A GRCh38
NC_000004.11:g.103422512G>A , CM000666.1:g.103422512G>A GRCh37
NC_000004.10:g.103641544G>A NCBI36
NG_050628.1:g.5027G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000507079.6:c.-487G>A ENSP00000426147.2:n.-487G>A
ENST00000226574.8:c.-441G>A ENSP00000226574.4:n.-441G>A
ENST00000394820.8:c.-441G>A ENSP00000378297.4:n.-441G>A
NM_001165412.1:c.-441G>A NP_001158884.1:n.-441G>A
NM_003998.3:c.-441G>A NP_003989.2:n.-441G>A
XM_011532467.1:c.537C>T XP_011530769.1:p.Leu179=
NR_136202.1:n.48+1084C>T
XM_024454067.1:c.-487G>A XP_024309835.1:n.-487G>A
XM_024454069.1:c.-487G>A XP_024309837.1:n.-487G>A
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