Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.139562096T= , CM000685.2:g.139562096T= | GRCh38 |
| NC_000023.10:g.138644255T= , CM000685.1:g.138644255T= | GRCh37 |
| NC_000023.9:g.138471921T= | NCBI36 |
| NG_007994.1:g.36361T= , LRG_556:g.36361T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218099.7:c.*25T= MANE Select | ENSP00000218099.2:n.*25T= | |
| ENST00000643157.1:n.1723+355T= | ||
| ENST00000218099.6:c.*25T= | ENSP00000218099.2:n.*25T= | |
| NM_000133.3:c.*25T= , LRG_556t1:c.*25T= | NP_000124.1:n.*25T= | |
| NM_001313913.1:c.*25T= | NP_001300842.1:n.*25T= | |
| XM_005262397.3:c.*25T= | XP_005262454.1:n.*25T= | |
| XM_005262397.4:c.*25T= | XP_005262454.1:n.*25T= | |
| NM_000133.4:c.*25T= MANE Select | NP_000124.1:n.*25T= | |
| NM_001313913.2:c.*25T= | NP_001300842.1:n.*25T= |