Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.70439131T= , CM000663.2:g.70439131T= | GRCh38 |
| NC_000001.10:g.70904814T= , CM000663.1:g.70904814T= | GRCh37 |
| NC_000001.9:g.70677402T= | NCBI36 |
| NG_008041.1:g.32860T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000370938.8:c.*4T= MANE Select | ENSP00000359976.3:n.*4T= | |
| ENST00000346806.2:c.*4T= | ENSP00000311554.2:n.*4T= | |
| ENST00000370938.7:c.*4T= | ENSP00000359976.3:n.*4T= | |
| ENST00000411986.6:c.*4T= | ENSP00000413407.2:n.*4T= | |
| ENST00000482383.1:n.497T= | ||
| NM_001190463.1:c.*4T= | NP_001177392.1:n.*4T= | |
| NM_001902.5:c.*4T= | NP_001893.2:n.*4T= | |
| NM_153742.4:c.*4T= | NP_714964.2:n.*4T= | |
| XM_005270509.2:c.*4T= | XP_005270566.1:n.*4T= | |
| XM_011540787.1:c.*4T= | XP_011539089.1:n.*4T= | |
| XM_005270509.3:c.*4T= | XP_005270566.1:n.*4T= | |
| XM_017000416.2:c.*4T= | XP_016855905.1:n.*4T= | |
| NM_001902.6:c.*4T= MANE Select | NP_001893.2:n.*4T= | |
| NM_001190463.2:c.*4T= | NP_001177392.1:n.*4T= | |
| NM_153742.5:c.*4T= | NP_714964.2:n.*4T= |