Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.6872663A>G , CM000686.2:g.6872663A>G | GRCh38 |
| NC_000024.9:g.6740704A>G , CM000686.1:g.6740704A>G | GRCh37 |
| NC_000024.8:g.6800704A>G | NCBI36 |
| NG_008011.1:g.6365T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001143.2:c.-12-43T>C MANE Select | NP_001134.1:n.-12-43T>C |
| ENST00000651267.2:c.-12-43T>C MANE Select | ENSP00000498344.1:n.-12-43T>C |
| NM_001143.1:c.-12-43T>C | NP_001134.1:n.-12-43T>C |
| NM_001364814.1:c.-12-43T>C | NP_001351743.1:n.-12-43T>C |
| ENST00000215479.10:c.-12-43T>C | ENSP00000215479.5:n.-12-43T>C |
| ENST00000215479.9:c.-12-43T>C | ENSP00000215479.5:n.-12-43T>C |
| ENST00000651267.1:c.-12-43T>C | ENSP00000498344.1:n.-12-43T>C |
| XM_011531472.1:c.-12-43T>C | XP_011529774.1:n.-12-43T>C |