Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.68667984T>C , CM000666.2:g.68667984T>C | GRCh38 |
| NC_000004.11:g.69533702T>C , CM000666.1:g.69533702T>C | GRCh37 |
| NC_000004.10:g.69216297T>C | NCBI36 |
| NG_052676.1:g.7793A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001076.4:c.873+56A>G MANE Select | NP_001067.2:n.873+56A>G |
| ENST00000338206.6:c.873+56A>G MANE Select | ENSP00000341045.5:n.873+56A>G |
| NM_001076.3:c.873+56A>G | NP_001067.2:n.873+56A>G |
| ENST00000338206.5:c.873+56A>G | ENSP00000341045.5:n.873+56A>G |
| ENST00000616841.4:c.873+56A>G | ENSP00000482004.1:n.873+56A>G |