Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150992947C>T , CM000669.2:g.150992947C>T | GRCh38 |
| NC_000007.13:g.150690035C>T , CM000669.1:g.150690035C>T | GRCh37 |
| NC_000007.12:g.150320968C>T | NCBI36 |
| NG_011992.1:g.6889C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297494.8:c.-51-806C>T MANE Select | ENSP00000297494.3:n.-51-806C>T | |
| ENST00000297494.7:c.-51-806C>T | ENSP00000297494.3:n.-51-806C>T | |
| ENST00000461406.5:c.-149+1647C>T | ENSP00000417143.1:n.-149+1647C>T | |
| NM_000603.4:c.-51-806C>T | NP_000594.2:n.-51-806C>T | |
| NM_000603.5:c.-51-806C>T MANE Select | NP_000594.2:n.-51-806C>T |