Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.20778627G>T , CM000686.2:g.20778627G>T | GRCh38 |
| NC_000024.9:g.22940513G>T , CM000686.1:g.22940513G>T | GRCh37 |
| NC_000024.8:g.21349901G>T | NCBI36 |
| NG_032924.1:g.27560G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001039567.3:c.533-882G>T MANE Select | NP_001034656.1:n.533-882G>T |
| ENST00000629237.2:c.533-882G>T MANE Select | ENSP00000486252.1:n.533-882G>T |
| NM_001039567.2:c.533-882G>T | NP_001034656.1:n.533-882G>T |
| ENST00000629237.1:c.533-882G>T | ENSP00000486252.1:n.533-882G>T |
| XM_011531423.1:c.482-882G>T | XP_011529725.1:n.482-882G>T |