Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.6872758A>T , CM000686.2:g.6872758A>T | GRCh38 |
| NC_000024.9:g.6740799A>T , CM000686.1:g.6740799A>T | GRCh37 |
| NC_000024.8:g.6800799A>T | NCBI36 |
| NG_008011.1:g.6270T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651267.2:c.-12-138T>A MANE Select | ENSP00000498344.1:n.-12-138T>A | |
| ENST00000215479.10:c.-12-138T>A | ENSP00000215479.5:n.-12-138T>A | |
| ENST00000651267.1:c.-12-138T>A | ENSP00000498344.1:n.-12-138T>A | |
| ENST00000215479.9:c.-12-138T>A | ENSP00000215479.5:n.-12-138T>A | |
| NM_001143.1:c.-12-138T>A | NP_001134.1:n.-12-138T>A | |
| XM_011531472.1:c.-12-138T>A | XP_011529774.1:n.-12-138T>A | |
| NM_001364814.1:c.-12-138T>A | NP_001351743.1:n.-12-138T>A | |
| NM_001143.2:c.-12-138T>A MANE Select | NP_001134.1:n.-12-138T>A |