Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.16992989C= , CM000670.2:g.16992989C= | GRCh38 |
| NC_000008.10:g.16850498C= , CM000670.1:g.16850498C= | GRCh37 |
| NC_000008.9:g.16894869C= | NCBI36 |
| NG_015978.1:g.14177G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_019851.3:c.*83G= MANE Select | NP_062825.1:n.*83G= |
| ENST00000180166.6:c.*83G= MANE Select | ENSP00000180166.5:n.*83G= |
| NM_019851.2:c.*83G= | NP_062825.1:n.*83G= |
| ENST00000180166.5:c.*83G= | ENSP00000180166.5:n.*83G= |
| ENST00000519941.1:c.423G= |