Linked Data
gnomAD v4:
1-193122110-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.193122110A>G , CM000663.2:g.193122110A>G | GRCh38 |
| NC_000001.10:g.193091240A>G , CM000663.1:g.193091240A>G | GRCh37 |
| NC_000001.9:g.191357863A>G | NCBI36 |
| NG_012691.1:g.5153A>G , LRG_507:g.5153A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367435.5:c.-91A>G MANE Select | ENSP00000356405.4:n.-91A>G | |
| ENST00000643006.1:c.-91A>G | ENSP00000496633.1:n.-91A>G | |
| ENST00000649895.1:n.128A>G | ||
| ENST00000650197.1:c.-91A>G | ENSP00000496929.1:n.-91A>G | |
| ENST00000367435.3:c.-91A>G | ENSP00000356405.3:n.-91A>G | |
| NM_024529.4:c.-91A>G , LRG_507t1:c.-91A>G | NP_078805.3:n.-91A>G | |
| XM_006711537.2:c.-91A>G | XP_006711600.1:n.-91A>G | |
| XM_006711537.4:c.-91A>G | XP_006711600.1:n.-91A>G | |
| XR_001738350.1:n.1547T>C | ||
| NM_024529.5:c.-91A>G MANE Select | NP_078805.3:n.-91A>G |