Linked Data
gnomAD v4:
15-44711343-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.44711343C>A , CM000677.2:g.44711343C>A | GRCh38 |
| NC_000015.9:g.45003541C>A , CM000677.1:g.45003541C>A | GRCh37 |
| NC_000015.8:g.42790833C>A | NCBI36 |
| NG_012920.1:g.4857C>A | |
| NG_012920.2:g.4867C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011521338.1:c.-577G>T | XP_011519640.1:n.-577G>T | |
| XM_011521339.1:c.-458G>T | XP_011519641.1:n.-458G>T | |
| XM_011521340.1:c.-399G>T | XP_011519642.1:n.-399G>T | |
| XM_011521343.1:c.-661G>T | XP_011519645.1:n.-661G>T | |
| XM_011521345.1:c.-632G>T | XP_011519647.1:n.-632G>T | |
| XM_011521338.3:c.-577G>T | XP_011519640.1:n.-577G>T | |
| XM_011521339.3:c.-458G>T | XP_011519641.1:n.-458G>T | |
| XM_011521340.3:c.-399G>T | XP_011519642.1:n.-399G>T | |
| XM_011521343.3:c.-661G>T | XP_011519645.1:n.-661G>T | |
| XM_011521345.3:c.-632G>T | XP_011519647.1:n.-632G>T | |
| NM_001387260.1:c.-87G>T | NP_001374189.1:n.-87G>T |