Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.146339494T>A , CM000667.2:g.146339494T>A | GRCh38 |
| NC_000005.9:g.145719057T>A , CM000667.1:g.145719057T>A | GRCh37 |
| NC_000005.8:g.145699250T>A | NCBI36 |
| NG_011885.1:g.5471T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000646991.2:c.121-54T>A MANE Select | ENSP00000495718.1:n.121-54T>A | |
| ENST00000230732.4:c.121-54T>A | ENSP00000230732.4:n.121-54T>A | |
| NM_002700.2:c.121-54T>A | NP_002691.1:n.121-54T>A | |
| NM_002700.3:c.121-54T>A MANE Select | NP_002691.1:n.121-54T>A |