Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.14871616T>C , CM000667.2:g.14871616T>C | GRCh38 |
| NC_000005.9:g.14871725T>C , CM000667.1:g.14871725T>C | GRCh37 |
| NC_000005.8:g.14924725T>C | NCBI36 |
| NG_008273.1:g.5163A>G | |
| NG_008273.2:g.5170A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000284268.8:c.-169A>G MANE Select | ENSP00000284268.6:n.-169A>G | |
| ENST00000284268.6:c.-169A>G | ENSP00000284268.6:n.-169A>G | |
| ENST00000505140.1:c.-169A>G | ENSP00000426332.1:n.-169A>G | |
| NM_054027.4:c.-169A>G | NP_473368.1:n.-169A>G | |
| XM_011514067.1:c.-169A>G | XP_011512369.1:n.-169A>G | |
| NM_054027.5:c.-169A>G | NP_473368.1:n.-169A>G | |
| NM_054027.6:c.-169A>G MANE Select | NP_473368.1:n.-169A>G |