Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.2251466C>G , CM000681.2:g.2251466C>G | GRCh38 |
| NC_000019.9:g.2251465C>G , CM000681.1:g.2251465C>G | GRCh37 |
| NC_000019.8:g.2202465C>G | NCBI36 |
| NG_012190.1:g.7353C>G | |
| NG_032853.1:g.9958G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221496.5:c.1192C>G MANE Select | ENSP00000221496.2:p.Pro398Ala | |
| ENST00000221496.4:c.1192C>G | ENSP00000221496.2:p.Pro398Ala | |
| ENST00000589313.2:n.1545C>G | ||
| NM_000479.3:c.1192C>G | NP_000470.2:p.Pro398Ala | |
| NM_000479.4:c.1192C>G | NP_000470.2:p.Pro398Ala | |
| NM_000479.5:c.1192C>G MANE Select | NP_000470.3:p.Pro398Ala |