Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38401307C>T , CM000685.2:g.38401307C>T | GRCh38 |
| NC_000023.10:g.38260560C>T , CM000685.1:g.38260560C>T | GRCh37 |
| NC_000023.9:g.38145504C>T | NCBI36 |
| NG_008471.1:g.53825C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000531.6:c.419C>T MANE Select | NP_000522.3:p.Ala140Val |
| ENST00000039007.5:c.419C>T MANE Select | ENSP00000039007.4:p.Ala140Val |
| NM_000531.5:c.419C>T | NP_000522.3:p.Ala140Val |
| ENST00000039007.4:c.419C>T | ENSP00000039007.4:p.Ala140Val |
| ENST00000465127.1:c.172-264814C>T | ENSP00000417050.1:n.172-264814C>T |
| ENST00000488812.1:n.456C>T | |
| ENST00000643344.1:c.*169C>T | ENSP00000496606.1:n.*169C>T |
| XM_017029556.1:c.419C>T | XP_016885045.1:p.Ala140Val |