Canonical Allele Identifier: CA103122908
Gene: NFKB1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1585215

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102523317T>C , CM000666.2:g.102523317T>C GRCh38
NC_000004.11:g.103444474T>C , CM000666.1:g.103444474T>C GRCh37
NC_000004.10:g.103663504T>C NCBI36
NG_050628.1:g.26989T>C

Transcript Alleles

HGVS Amino-acid change
NM_001165412.1:c.-7-2195T>C VV NP_001158884.1:p.=
NM_003998.3:c.-7-2195T>C VV NP_003989.2:p.=
XM_011532006.1:c.18-2195T>C XP_011530308.1:p.=
XM_011532007.1:c.-7-2195T>C XP_011530309.1:p.=
NM_001319226.1:c.-7-2195T>C VV NP_001306155.1:p.=
XM_011532006.2:c.18-2195T>C XP_011530308.1:p.=
XM_024454067.1:c.18-2195T>C XP_024309835.1:p.=
XM_024454068.1:c.-7-2195T>C XP_024309836.1:p.=
XM_024454069.1:c.18-2195T>C XP_024309837.1:p.=
NM_003998.4:c.-7-2195T>C VV MANE Preferred NP_003989.2:p.=
ENST00000226574.8:c.-7-2195T>C ENSP00000226574.4:p.=
ENST00000394820.8:c.-7-2195T>C ENSP00000378297.4:p.=
ENST00000505458.5:c.-7-2195T>C ENSP00000424790.1:p.=
ENST00000507079.5:c.18-2195T>C ENSP00000426147.1:p.=
ENST00000509165.1:c.-7-2195T>C ENSP00000423877.1:p.=
ENST00000511926.5:c.18-2195T>C ENSP00000420904.1:p.=