Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46009497T= , CM000682.2:g.46009497T= | GRCh38 |
| NC_000020.10:g.44638136T= , CM000682.1:g.44638136T= | GRCh37 |
| NC_000020.9:g.44071543T= | NCBI36 |
| NG_011468.1:g.5590T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004994.3:c.139-369T= MANE Select | NP_004985.2:n.139-369T= |
| ENST00000372330.3:c.139-369T= MANE Select | ENSP00000361405.3:n.139-369T= |
| NM_004994.2:c.139-369T= | NP_004985.2:n.139-369T= |