Linked Data
gnomAD v4:
3-186842734-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.186842734G>T , CM000665.2:g.186842734G>T | GRCh38 |
| NC_000003.11:g.186560523G>T , CM000665.1:g.186560523G>T | GRCh37 |
| NC_000003.10:g.188043217G>T | NCBI36 |
| NG_021140.1:g.5061G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320741.7:c.-24G>T MANE Select | ENSP00000320709.2:n.-24G>T | |
| ENST00000320741.6:c.-24G>T | ENSP00000320709.2:n.-24G>T | |
| ENST00000444204.2:c.-75G>T | ENSP00000389814.2:n.-75G>T | |
| NM_001177800.1:c.-75G>T | NP_001171271.1:n.-75G>T | |
| NM_004797.3:c.-24G>T | NP_004788.1:n.-24G>T | |
| XM_011513324.1:c.-140G>T | XP_011511626.1:n.-140G>T | |
| NM_004797.4:c.-24G>T MANE Select | NP_004788.1:n.-24G>T | |
| NM_001177800.2:c.-75G>T | NP_001171271.1:n.-75G>T |