Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38411890C>T , CM000685.2:g.38411890C>T | GRCh38 |
| NC_000023.10:g.38271143C>T , CM000685.1:g.38271143C>T | GRCh37 |
| NC_000023.9:g.38156087C>T | NCBI36 |
| NG_008471.1:g.64408C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000531.6:c.896C>T MANE Select | NP_000522.3:p.Thr299Ile |
| ENST00000039007.5:c.896C>T MANE Select | ENSP00000039007.4:p.Thr299Ile |
| NM_000531.5:c.896C>T | NP_000522.3:p.Thr299Ile |
| ENST00000039007.4:c.896C>T | ENSP00000039007.4:p.Thr299Ile |
| ENST00000465127.1:c.172-254231C>T | ENSP00000417050.1:n.172-254231C>T |
| ENST00000643344.1:c.*646C>T | ENSP00000496606.1:n.*646C>T |