Linked Data
gnomAD v4:
20-33443701-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.33443701A>T , CM000682.2:g.33443701A>T | GRCh38 |
| NC_000020.10:g.32031507A>T , CM000682.1:g.32031507A>T | GRCh37 |
| NC_000020.9:g.31495168A>T | NCBI36 |
| NG_011622.1:g.5192T>A , LRG_332:g.5192T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000217381.3:c.-81T>A MANE Select | ENSP00000217381.2:n.-81T>A | |
| ENST00000217381.2:c.-81T>A | ENSP00000217381.2:n.-81T>A | |
| NM_003098.2:c.-81T>A , LRG_332t1:c.-81T>A | NP_003089.1:n.-81T>A | |
| XM_005260517.1:c.-81T>A | XP_005260574.1:n.-81T>A | |
| XM_011529007.1:c.-81T>A | XP_011527309.1:n.-81T>A | |
| XM_011529008.1:c.-81T>A | XP_011527310.1:n.-81T>A | |
| XR_936612.1:n.153T>A | ||
| NM_003098.3:c.-81T>A MANE Select | NP_003089.1:n.-81T>A |