Linked Data
gnomAD v4:
13-27924779-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.27924779G>A , CM000675.2:g.27924779G>A | GRCh38 |
| NC_000013.10:g.28498916G>A , CM000675.1:g.28498916G>A | GRCh37 |
| NC_000013.9:g.27396916G>A | NCBI36 |
| NG_008183.1:g.9749G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381033.5:c.*78G>A MANE Select | ENSP00000370421.4:n.*78G>A | |
| ENST00000381033.4:c.*78G>A | ENSP00000370421.4:n.*78G>A | |
| NM_000209.3:c.*78G>A | NP_000200.1:n.*78G>A | |
| NM_000209.4:c.*78G>A MANE Select | NP_000200.1:n.*78G>A |