Linked Data
gnomAD v4:
15-44711353-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.44711353T>A , CM000677.2:g.44711353T>A | GRCh38 |
| NC_000015.9:g.45003551T>A , CM000677.1:g.45003551T>A | GRCh37 |
| NC_000015.8:g.42790843T>A | NCBI36 |
| NG_012920.1:g.4867T>A | |
| NG_012920.2:g.4877T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011521338.1:c.-587A>T | XP_011519640.1:n.-587A>T | |
| XM_011521339.1:c.-468A>T | XP_011519641.1:n.-468A>T | |
| XM_011521340.1:c.-409A>T | XP_011519642.1:n.-409A>T | |
| XM_011521343.1:c.-671A>T | XP_011519645.1:n.-671A>T | |
| XM_011521345.1:c.-642A>T | XP_011519647.1:n.-642A>T | |
| XM_011521338.3:c.-587A>T | XP_011519640.1:n.-587A>T | |
| XM_011521339.3:c.-468A>T | XP_011519641.1:n.-468A>T | |
| XM_011521340.3:c.-409A>T | XP_011519642.1:n.-409A>T | |
| XM_011521343.3:c.-671A>T | XP_011519645.1:n.-671A>T | |
| XM_011521345.3:c.-642A>T | XP_011519647.1:n.-642A>T | |
| NM_001387260.1:c.-97A>T | NP_001374189.1:n.-97A>T |