Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.15930578T= , CM000663.2:g.15930578T= | GRCh38 |
| NC_000001.10:g.16257073T= , CM000663.1:g.16257073T= | GRCh37 |
| NC_000001.9:g.16129660T= | NCBI36 |
| NG_050663.1:g.87715T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000438066.2:c.*5189T= | ENSP00000388021.2:n.*5189T= | |
| ENST00000375759.8:c.4338T= MANE Select | ENSP00000364912.3:p.Ala1446= | |
| ENST00000375759.7:c.4338T= | ENSP00000364912.3:p.Ala1446= | |
| NM_015001.2:c.4338T= | NP_055816.2:p.Ala1446= | |
| NM_015001.3:c.4338T= MANE Select | NP_055816.2:p.Ala1446= |