Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8080978T>C , CM000679.2:g.8080978T>C | GRCh38 |
| NC_000017.10:g.7984296T>C , CM000679.1:g.7984296T>C | GRCh37 |
| NC_000017.9:g.7925021T>C | NCBI36 |
| NG_007099.1:g.11726A>G | |
| NG_007099.2:g.11739A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001139.3:c.435-2A>G MANE Select | NP_001130.1:n.435-2A>G |
| ENST00000647874.1:c.435-2A>G MANE Select | ENSP00000497784.1:n.435-2A>G |
| NM_001139.2:c.435-2A>G | NP_001130.1:n.435-2A>G |
| ENST00000319144.4:c.435-2A>G | ENSP00000315167.4:n.435-2A>G |
| XR_001752778.1:n.1207T>C |