Linked Data
gnomAD v4:
11-6390439-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6390439A>C , CM000673.2:g.6390439A>C | GRCh38 |
| NC_000011.9:g.6411669A>C , CM000673.1:g.6411669A>C | GRCh37 |
| NC_000011.8:g.6368245A>C | NCBI36 |
| NG_011780.1:g.5015A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342245.8:c.-160A>C | ENSP00000340409.4:n.-160A>C | |
| NM_000543.4:c.-160A>C | NP_000534.3:n.-160A>C | |
| NM_001007593.2:c.-160A>C | NP_001007594.2:n.-160A>C | |
| XM_005253075.3:c.-160A>C | XP_005253132.1:n.-160A>C | |
| XM_011520303.1:c.-160A>C | XP_011518605.1:n.-160A>C | |
| XM_011520304.1:c.-160A>C | XP_011518606.1:n.-160A>C | |
| XR_930886.1:n.139A>C | ||
| NM_001318087.1:c.-160A>C | NP_001305016.1:n.-160A>C | |
| NM_001318088.1:c.-1121A>C | NP_001305017.1:n.-1121A>C | |
| NR_027400.2:n.26A>C | ||
| NR_134502.1:n.26A>C |