HGVS | Genome Assembly |
---|---|
NC_000006.12:g.44258458T>C , CM000668.2:g.44258458T>C | GRCh38 |
NC_000006.11:g.44226195T>C , CM000668.1:g.44226195T>C | GRCh37 |
NC_000006.10:g.44334173T>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000619360.6:c.*761A>G (NFKBIE) MANE Select | ENSP00000480216.1:n.*761A>G | |
ENST00000275015.9:c.*761A>G (NFKBIE) | ENSP00000275015.3:n.*761A>G | |
ENST00000619360.4:c.*761A>G (NFKBIE) | ENSP00000480216.1:n.*761A>G | |
NM_004556.2:c.*761A>G (NFKBIE) | NP_004547.2:n.*761A>G | |
NM_004556.3:c.*761A>G (NFKBIE) MANE Select | NP_004547.3:n.*761A>G | |
NM_001318876.2:c.946-183432T>C (POLR1C) | NP_001305805.1:n.946-183432T>C |