Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.193122108G>A , CM000663.2:g.193122108G>A | GRCh38 |
| NC_000001.10:g.193091238G>A , CM000663.1:g.193091238G>A | GRCh37 |
| NC_000001.9:g.191357861G>A | NCBI36 |
| NG_012691.1:g.5151G>A , LRG_507:g.5151G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367435.5:c.-93G>A MANE Select | ENSP00000356405.4:n.-93G>A | |
| ENST00000643006.1:c.-93G>A | ENSP00000496633.1:n.-93G>A | |
| ENST00000649895.1:n.126G>A | ||
| ENST00000650197.1:c.-93G>A | ENSP00000496929.1:n.-93G>A | |
| ENST00000367435.3:c.-93G>A | ENSP00000356405.3:n.-93G>A | |
| NM_024529.4:c.-93G>A , LRG_507t1:c.-93G>A | NP_078805.3:n.-93G>A | |
| XM_006711537.2:c.-93G>A | XP_006711600.1:n.-93G>A | |
| XM_006711537.4:c.-93G>A | XP_006711600.1:n.-93G>A | |
| XR_001738350.1:n.1549C>T | ||
| NM_024529.5:c.-93G>A MANE Select | NP_078805.3:n.-93G>A |