Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.27750759A>C , CM000684.2:g.27750759A>C | GRCh38 |
| NC_000022.10:g.28146747A>C , CM000684.1:g.28146747A>C | GRCh37 |
| NC_000022.9:g.26476747A>C | NCBI36 |
| NG_023258.1:g.55740T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703102.1:n.644T>G | ||
| ENST00000302326.5:c.*156T>G MANE Select | ENSP00000304956.4:n.*156T>G | |
| ENST00000302326.4:c.*156T>G | ENSP00000304956.4:n.*156T>G | |
| ENST00000424656.1:c.455+17T>G | ||
| ENST00000497225.1:n.475T>G | ||
| NM_002430.2:c.*156T>G | NP_002421.3:n.*156T>G | |
| NM_002430.3:c.*156T>G MANE Select | NP_002421.3:n.*156T>G |