Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.68646651A>T , CM000666.2:g.68646651A>T | GRCh38 |
| NC_000004.11:g.69512369A>T , CM000666.1:g.69512369A>T | GRCh37 |
| NC_000004.10:g.69194964A>T | NCBI36 |
| NG_052676.1:g.29126T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338206.6:c.*453T>A MANE Select | ENSP00000341045.5:n.*453T>A | |
| ENST00000338206.5:c.*453T>A | ENSP00000341045.5:n.*453T>A | |
| ENST00000616841.4:c.1732+314T>A | ENSP00000482004.1:n.1732+314T>A | |
| NM_001076.3:c.*453T>A | NP_001067.2:n.*453T>A | |
| NM_001076.4:c.*453T>A MANE Select | NP_001067.2:n.*453T>A |