Linked Data
gnomAD v4:
13-53051647-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.53051647A>G , CM000675.2:g.53051647A>G | GRCh38 |
| NC_000013.10:g.53625782A>G , CM000675.1:g.53625782A>G | GRCh37 |
| NC_000013.9:g.52523783A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000219022.3:c.*876A>G MANE Select | ENSP00000219022.2:n.*876A>G | |
| ENST00000219022.2:c.*876A>G | ENSP00000219022.2:n.*876A>G | |
| NM_006418.4:c.*876A>G | NP_006409.3:n.*876A>G | |
| NM_006418.5:c.*876A>G MANE Select | NP_006409.3:n.*876A>G |