Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.66228150T= , CM000679.2:g.66228150T= | GRCh38 |
| NC_000017.10:g.64224268T= , CM000679.1:g.64224268T= | GRCh37 |
| NC_000017.9:g.61654730T= | NCBI36 |
| NG_012045.1:g.6289A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000205948.11:c.111A= MANE Select | ENSP00000205948.6:p.Leu37= | |
| ENST00000205948.10:c.111A= | ENSP00000205948.6:p.Leu37= | |
| ENST00000577982.1:c.111A= | ENSP00000464301.1:p.Leu37= | |
| ENST00000581797.5:c.-70A= | ENSP00000463553.1:n.-70A= | |
| NM_000042.2:c.111A= | NP_000033.2:p.Leu37= | |
| NM_000042.3:c.111A= MANE Select | NP_000033.2:p.Leu37= |