Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.3082965C>G , CM000682.2:g.3082965C>G | GRCh38 |
| NC_000020.10:g.3063611C>G , CM000682.1:g.3063611C>G | GRCh37 |
| NC_000020.9:g.3011611C>G | NCBI36 |
| NG_008663.1:g.6760G>C , LRG_715:g.6760G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380293.3:c.322+12G>C MANE Select | ENSP00000369647.3:n.322+12G>C | |
| NM_000490.4:c.322+12G>C , LRG_715t1:c.322+12G>C | NP_000481.2:n.322+12G>C | |
| XM_011529267.1:c.322+12G>C | XP_011527569.1:n.322+12G>C | |
| XM_011529267.2:c.322+12G>C | XP_011527569.1:n.322+12G>C | |
| NM_000490.5:c.322+12G>C MANE Select | NP_000481.2:n.322+12G>C |