Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.80286734A= , CM000666.2:g.80286734A= | GRCh38 |
| NC_000004.11:g.81207888A= , CM000666.1:g.81207888A= | GRCh37 |
| NC_000004.10:g.81426912A= | NCBI36 |
| NG_029501.1:g.25147A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000312465.12:c.*62A= MANE Select | ENSP00000311697.7:n.*62A= | |
| ENST00000312465.11:c.*62A= | ENSP00000311697.7:n.*62A= | |
| ENST00000456523.3:c.*393A= | ENSP00000398353.3:n.*393A= | |
| ENST00000503413.1:n.818A= | ||
| ENST00000507780.1:c.342+11722A= | ENSP00000423903.1:n.342+11722A= | |
| NM_001291812.1:c.*62A= | NP_001278741.1:n.*62A= | |
| NM_004464.3:c.*62A= | NP_004455.2:n.*62A= | |
| NM_033143.2:c.*393A= | NP_149134.1:n.*393A= | |
| NM_001291812.2:c.*62A= | NP_001278741.1:n.*62A= | |
| NM_004464.4:c.*62A= MANE Select | NP_004455.2:n.*62A= |