Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.147900074T= , CM000669.2:g.147900074T= | GRCh38 |
| NC_000007.13:g.147597166T= , CM000669.1:g.147597166T= | GRCh37 |
| NC_000007.12:g.147228099T= | NCBI36 |
| NG_007092.2:g.1788714T= | |
| NG_007092.3:g.1789074T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_014141.6:c.2099-3491T= MANE Select | NP_054860.1:n.2099-3491T= |
| ENST00000361727.8:c.2099-3491T= MANE Select | ENSP00000354778.3:n.2099-3491T= |
| NM_014141.5:c.2099-3491T= | NP_054860.1:n.2099-3491T= |
| ENST00000361727.7:c.2099-3491T= | ENSP00000354778.3:n.2099-3491T= |
| ENST00000455301.2:n.34-3491T= | |
| ENST00000627772.2:n.272-3491T= | |
| ENST00000636755.1:n.45+3001T= | |
| ENST00000636870.1:n.1961-3491T= | |
| ENST00000637654.1:n.63-3491T= | |
| ENST00000637825.1:n.1582-3491T= | |
| XM_006715919.1:c.587-3491T= | XP_006715982.1:n.587-3491T= |