Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.2250745C>T , CM000681.2:g.2250745C>T | GRCh38 |
| NC_000019.9:g.2250744C>T , CM000681.1:g.2250744C>T | GRCh37 |
| NC_000019.8:g.2201744C>T | NCBI36 |
| NG_012190.1:g.6632C>T | |
| NG_032853.1:g.10679G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000479.5:c.649C>T MANE Select | NP_000470.3:p.Gln217Ter |
| ENST00000221496.5:c.649C>T MANE Select | ENSP00000221496.2:p.Gln217Ter |
| NM_000479.3:c.649C>T | NP_000470.2:p.Gln217Ter |
| NM_000479.4:c.649C>T | NP_000470.2:p.Gln217Ter |
| ENST00000221496.4:c.649C>T | ENSP00000221496.2:p.Gln217Ter |
| ENST00000589313.2:n.1002C>T | |
| ENST00000592877.1:n.530C>T |