Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8073215G= , CM000679.2:g.8073215G= | GRCh38 |
| NC_000017.10:g.7976533G= , CM000679.1:g.7976533G= | GRCh37 |
| NC_000017.9:g.7917258G= | NCBI36 |
| NG_007099.1:g.19489C= | |
| NG_007099.2:g.19502C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001139.3:c.1859C= MANE Select | NP_001130.1:p.Pro620= |
| ENST00000647874.1:c.1859C= MANE Select | ENSP00000497784.1:p.Pro620= |
| NM_001139.2:c.1859C= | NP_001130.1:p.Pro620= |
| ENST00000319144.4:c.1859C= | ENSP00000315167.4:p.Pro620= |
| ENST00000577351.5:n.583C= | |
| ENST00000649809.1:c.923C= | ENSP00000496845.1:p.Pro308= |
| ENST00000650441.1:n.282C= |