Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.141895250A= , CM000685.2:g.141895250A= | GRCh38 |
| NC_000023.10:g.140983036A= , CM000685.1:g.140983036A= | GRCh37 |
| NC_000023.9:g.140810702A= | NCBI36 |
| NG_013272.1:g.61935A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000298296.1:c.910-19A= MANE Select | ENSP00000298296.1:n.910-19A= | |
| ENST00000443323.2:c.-118-1181A= | ENSP00000438254.1:n.-118-1181A= | |
| ENST00000483584.5:n.150-19A= | ||
| ENST00000544766.5:c.-378-19A= | ENSP00000440444.1:n.-378-19A= | |
| NM_138702.1:c.910-19A= MANE Select | NP_619647.1:n.910-19A= | |
| NM_177456.2:c.-378-19A= | NP_803251.1:n.-378-19A= | |
| XM_011531267.1:c.-320A= | XP_011529569.1:n.-320A= | |
| XM_011531267.3:c.-320A= | XP_011529569.1:n.-320A= | |
| XM_017029265.2:c.-378-19A= | XP_016884754.1:n.-378-19A= |