Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.68646714A>C , CM000666.2:g.68646714A>C | GRCh38 |
| NC_000004.11:g.69512432A>C , CM000666.1:g.69512432A>C | GRCh37 |
| NC_000004.10:g.69195027A>C | NCBI36 |
| NG_052676.1:g.29063T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338206.6:c.*390T>G MANE Select | ENSP00000341045.5:n.*390T>G | |
| ENST00000338206.5:c.*390T>G | ENSP00000341045.5:n.*390T>G | |
| ENST00000616841.4:c.1732+251T>G | ENSP00000482004.1:n.1732+251T>G | |
| NM_001076.3:c.*390T>G | NP_001067.2:n.*390T>G | |
| NM_001076.4:c.*390T>G MANE Select | NP_001067.2:n.*390T>G |