Linked Data
gnomAD v4:
15-44711355-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.44711355A>G , CM000677.2:g.44711355A>G | GRCh38 |
| NC_000015.9:g.45003553A>G , CM000677.1:g.45003553A>G | GRCh37 |
| NC_000015.8:g.42790845A>G | NCBI36 |
| NG_012920.1:g.4869A>G | |
| NG_012920.2:g.4879A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011521338.1:c.-589T>C | XP_011519640.1:n.-589T>C | |
| XM_011521339.1:c.-470T>C | XP_011519641.1:n.-470T>C | |
| XM_011521340.1:c.-411T>C | XP_011519642.1:n.-411T>C | |
| XM_011521343.1:c.-673T>C | XP_011519645.1:n.-673T>C | |
| XM_011521345.1:c.-644T>C | XP_011519647.1:n.-644T>C | |
| XM_011521338.3:c.-589T>C | XP_011519640.1:n.-589T>C | |
| XM_011521339.3:c.-470T>C | XP_011519641.1:n.-470T>C | |
| XM_011521340.3:c.-411T>C | XP_011519642.1:n.-411T>C | |
| XM_011521343.3:c.-673T>C | XP_011519645.1:n.-673T>C | |
| XM_011521345.3:c.-644T>C | XP_011519647.1:n.-644T>C | |
| NM_001387260.1:c.-99T>C | NP_001374189.1:n.-99T>C |