Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.193122032C= , CM000663.2:g.193122032C= | GRCh38 |
| NC_000001.10:g.193091162C= , CM000663.1:g.193091162C= | GRCh37 |
| NC_000001.9:g.191357785C= | NCBI36 |
| NG_012691.1:g.5075C= , LRG_507:g.5075C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367435.5:c.-169C= MANE Select | ENSP00000356405.4:n.-169C= | |
| ENST00000643006.1:c.-169C= | ENSP00000496633.1:n.-169C= | |
| ENST00000649895.1:n.50C= | ||
| ENST00000367435.3:c.-169C= | ENSP00000356405.3:n.-169C= | |
| NM_024529.4:c.-169C= , LRG_507t1:c.-169C= | NP_078805.3:n.-169C= | |
| XM_006711537.4:c.-169C= | XP_006711600.1:n.-169C= | |
| XR_001738350.1:n.1625G= | ||
| NM_024529.5:c.-169C= MANE Select | NP_078805.3:n.-169C= |