Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46011053G= , CM000682.2:g.46011053G= | GRCh38 |
| NC_000020.10:g.44639692G= , CM000682.1:g.44639692G= | GRCh37 |
| NC_000020.9:g.44073099G= | NCBI36 |
| NG_011468.1:g.7146G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004994.3:c.649+3G= MANE Select | NP_004985.2:n.649+3G= |
| ENST00000372330.3:c.649+3G= MANE Select | ENSP00000361405.3:n.649+3G= |
| NM_004994.2:c.649+3G= | NP_004985.2:n.649+3G= |