Canonical Allele Identifier: CA440620675
Gene: NFKB1 HGNC NCBI

Linked Data

dbSNP Id: rs72696119
MyVariant Identifiers: chr4:g.103422504C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501347C>T , CM000666.2:g.102501347C>T GRCh38
NC_000004.11:g.103422504C>T , CM000666.1:g.103422504C>T GRCh37
NC_000004.10:g.103641536C>T NCBI36
NG_050628.1:g.5019C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000507079.6:c.-495C>T ENSP00000426147.2:n.-495C>T
ENST00000226574.8:c.-449C>T ENSP00000226574.4:n.-449C>T
ENST00000394820.8:c.-449C>T ENSP00000378297.4:n.-449C>T
NM_001165412.1:c.-449C>T NP_001158884.1:n.-449C>T
NM_003998.3:c.-449C>T NP_003989.2:n.-449C>T
XM_011532467.1:c.545G>A XP_011530769.1:p.Cys182Tyr
NR_136202.1:n.48+1092G>A
XM_024454067.1:c.-495C>T XP_024309835.1:n.-495C>T
XM_024454069.1:c.-495C>T XP_024309837.1:n.-495C>T