Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67483150G= , CM000673.2:g.67483150G= | GRCh38 |
| NC_000011.9:g.67250621G= , CM000673.1:g.67250621G= | GRCh37 |
| NC_000011.8:g.67007197G= | NCBI36 |
| NG_008969.1:g.5117G= , LRG_460:g.5117G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000528641.7:c.-9G= | ENSP00000434982.3:n.-9G= | |
| ENST00000682324.1:c.-9G= | ENSP00000508017.1:n.-9G= | |
| ENST00000682699.1:c.-9G= | ENSP00000507935.1:n.-9G= | |
| ENST00000683237.1:c.-9G= | ENSP00000507343.1:n.-9G= | |
| ENST00000684006.1:c.-9G= | ENSP00000507269.1:n.-9G= | |
| ENST00000684657.1:c.-9G= | ENSP00000507961.1:n.-9G= | |
| ENST00000279146.8:c.-9G= MANE Select | ENSP00000279146.3:n.-9G= | |
| ENST00000279146.7:c.-9G= | ENSP00000279146.3:n.-9G= | |
| ENST00000528641.6:c.-9G= | ENSP00000434982.2:n.-9G= | |
| ENST00000529797.1:n.102G= | ||
| NM_001302960.1:c.-9G= | NP_001289889.1:n.-9G= | |
| NM_003977.3:c.-9G= | NP_003968.3:n.-9G= | |
| XM_024448761.1:c.-9G= | XP_024304529.1:n.-9G= | |
| NM_003977.4:c.-9G= MANE Select | NP_003968.3:n.-9G= | |
| NM_001302960.2:c.-9G= | NP_001289889.1:n.-9G= |