Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.68647050A>G , CM000666.2:g.68647050A>G | GRCh38 |
| NC_000004.11:g.69512768A>G , CM000666.1:g.69512768A>G | GRCh37 |
| NC_000004.10:g.69195363A>G | NCBI36 |
| NG_052676.1:g.28727T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338206.6:c.*54T>C MANE Select | ENSP00000341045.5:n.*54T>C | |
| ENST00000338206.5:c.*54T>C | ENSP00000341045.5:n.*54T>C | |
| ENST00000616841.4:c.1647T>C | ENSP00000482004.1:n.1647T>C | |
| NM_001076.3:c.*54T>C | NP_001067.2:n.*54T>C | |
| NM_001076.4:c.*54T>C MANE Select | NP_001067.2:n.*54T>C |