Linked Data
gnomAD v4:
4-71784129-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.71784129A>T , CM000666.2:g.71784129A>T | GRCh38 |
| NC_000004.11:g.72649846A>T , CM000666.1:g.72649846A>T | GRCh37 |
| NC_000004.10:g.72868710A>T | NCBI36 |
| NG_012837.2:g.26392T>A | |
| NG_012837.3:g.26392T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000273951.12:c.-111T>A | ENSP00000273951.8:n.-111T>A | |
| ENST00000504199.5:c.22-75T>A | ENSP00000421725.1:n.22-75T>A | |
| ENST00000506245.1:c.-36-75T>A | ENSP00000426718.1:n.-36-75T>A | |
| NM_000583.3:c.-111T>A | NP_000574.2:n.-111T>A | |
| NM_001204306.1:c.-36-75T>A | NP_001191235.1:n.-36-75T>A | |
| NM_001204307.1:c.22-75T>A | NP_001191236.1:n.22-75T>A | |
| XM_006714177.2:c.-111T>A | XP_006714240.1:n.-111T>A |