Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.77268546C= , CM000680.2:g.77268546C= | GRCh38 |
| NC_000018.9:g.74980502C= , CM000680.1:g.74980502C= | GRCh37 |
| NC_000018.8:g.73109490C= | NCBI36 |
| NG_009223.1:g.23495C= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000299727.5:c.733-39C= MANE Select | ENSP00000299727.3:n.733-39C= | |
| ENST00000299727.4:c.733-39C= | ENSP00000299727.3:n.733-39C= | |
| NM_001480.3:c.733-39C= | NP_001471.2:n.733-39C= | |
| NM_001480.4:c.733-39C= MANE Select | NP_001471.2:n.733-39C= |