Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.147491511A= , CM000669.2:g.147491511A= | GRCh38 |
| NC_000007.13:g.147188603A= , CM000669.1:g.147188603A= | GRCh37 |
| NC_000007.12:g.146819536A= | NCBI36 |
| NG_007092.2:g.1380151A= | |
| NG_007092.3:g.1380511A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361727.8:c.1777+5470A= MANE Select | ENSP00000354778.3:n.1777+5470A= | |
| ENST00000636870.1:n.1639+5470A= | ||
| ENST00000637694.1:n.1681-5110A= | ||
| ENST00000637825.1:n.1260+5470A= | ||
| ENST00000638117.1:n.1680+5470A= | ||
| ENST00000361727.7:c.1777+5470A= | ENSP00000354778.3:n.1777+5470A= | |
| NM_014141.5:c.1777+5470A= | NP_054860.1:n.1777+5470A= | |
| XM_006715919.1:c.265+5470A= | XP_006715982.1:n.265+5470A= | |
| XM_017011950.2:c.1777+5470A= | XP_016867439.1:n.1777+5470A= | |
| NM_014141.6:c.1777+5470A= MANE Select | NP_054860.1:n.1777+5470A= |