Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46010332A= , CM000682.2:g.46010332A= | GRCh38 |
| NC_000020.10:g.44638971A= , CM000682.1:g.44638971A= | GRCh37 |
| NC_000020.9:g.44072378A= | NCBI36 |
| NG_011468.1:g.6425A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004994.3:c.372-151A= MANE Select | NP_004985.2:n.372-151A= |
| ENST00000372330.3:c.372-151A= MANE Select | ENSP00000361405.3:n.372-151A= |
| NM_004994.2:c.372-151A= | NP_004985.2:n.372-151A= |