Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133651448C= , CM000671.2:g.133651448C= | GRCh38 |
| NC_000009.11:g.136516570C= , CM000671.1:g.136516570C= | GRCh37 |
| NC_000009.10:g.135506391C= | NCBI36 |
| NG_008645.1:g.20086C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000787.4:c.1192-186C= MANE Select | NP_000778.3:n.1192-186C= |
| ENST00000393056.8:c.1192-186C= MANE Select | ENSP00000376776.2:n.1192-186C= |
| NM_000787.3:c.1192-186C= | NP_000778.3:n.1192-186C= |
| ENST00000393056.6:c.1192-186C= | ENSP00000376776.2:n.1192-186C= |