Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.43128256C>T , CM000672.2:g.43128256C>T | GRCh38 |
| NC_000010.10:g.43623704C>T , CM000672.1:g.43623704C>T | GRCh37 |
| NC_000010.9:g.42943710C>T | NCBI36 |
| NG_007489.1:g.56188C>T , LRG_518:g.56188C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_020975.6:c.3332C>T MANE Select | NP_066124.1:p.Thr1111Met |
| ENST00000355710.8:c.3332C>T MANE Select | ENSP00000347942.3:p.Thr1111Met |
| NM_020975.4:c.3332C>T , LRG_518t1:c.3332C>T | NP_066124.1:p.Thr1111Met |
| NM_020975.5:c.3332C>T | NP_066124.1:p.Thr1111Met |
| ENST00000355710.7:c.3332C>T | ENSP00000347942.3:p.Thr1111Met |
| ENST00000615310.4:c.*681C>T | ENSP00000480088.1:n.*681C>T |
| ENST00000615310.5:c.*1502C>T | ENSP00000480088.2:n.*1502C>T |
| ENST00000683007.1:n.4295C>T | |
| XM_011540027.1:c.3332C>T | XP_011538329.1:p.Thr1111Met |