Linked Data
gnomAD v4:
13-28659008-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.28659008C>A , CM000675.2:g.28659008C>A | GRCh38 |
| NC_000013.10:g.29233145C>A , CM000675.1:g.29233145C>A | GRCh37 |
| NC_000013.9:g.28131145C>A | NCBI36 |
| NG_027550.1:g.5005C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NM_015932.5:c.-177C>A | NP_057016.1:n.-177C>A |