Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.44258363C= , CM000668.2:g.44258363C= | GRCh38 |
| NC_000006.11:g.44226100C= , CM000668.1:g.44226100C= | GRCh37 |
| NC_000006.10:g.44334078C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000619360.6:c.*856G= (NFKBIE) MANE Select | ENSP00000480216.1:n.*856G= | |
| ENST00000275015.9:c.*856G= (NFKBIE) | ENSP00000275015.3:n.*856G= | |
| ENST00000619360.4:c.*856G= (NFKBIE) | ENSP00000480216.1:n.*856G= | |
| NM_004556.2:c.*856G= (NFKBIE) | NP_004547.2:n.*856G= | |
| NM_004556.3:c.*856G= (NFKBIE) MANE Select | NP_004547.3:n.*856G= | |
| NM_001318876.2:c.946-183527C= (POLR1C) | NP_001305805.1:n.946-183527C= |