Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38409052T= , CM000685.2:g.38409052T= | GRCh38 |
| NC_000023.10:g.38268305T= , CM000685.1:g.38268305T= | GRCh37 |
| NC_000023.9:g.38153249T= | NCBI36 |
| NG_008471.1:g.61570T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000039007.5:c.867+27T= MANE Select | ENSP00000039007.4:n.867+27T= | |
| ENST00000643344.1:c.*617+27T= | ENSP00000496606.1:n.*617+27T= | |
| ENST00000039007.4:c.867+27T= | ENSP00000039007.4:n.867+27T= | |
| ENST00000465127.1:c.172-257069T= | ENSP00000417050.1:n.172-257069T= | |
| NM_000531.5:c.867+27T= | NP_000522.3:n.867+27T= | |
| XM_017029556.1:c.867+27T= | XP_016885045.1:n.867+27T= | |
| NM_000531.6:c.867+27T= MANE Select | NP_000522.3:n.867+27T= |