Linked Data
gnomAD v4:
18-77268552-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.77268552C>G , CM000680.2:g.77268552C>G | GRCh38 |
| NC_000018.9:g.74980508C>G , CM000680.1:g.74980508C>G | GRCh37 |
| NC_000018.8:g.73109496C>G | NCBI36 |
| NG_009223.1:g.23501C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000299727.5:c.733-33C>G MANE Select | ENSP00000299727.3:n.733-33C>G | |
| ENST00000299727.4:c.733-33C>G | ENSP00000299727.3:n.733-33C>G | |
| NM_001480.3:c.733-33C>G | NP_001471.2:n.733-33C>G | |
| NM_001480.4:c.733-33C>G MANE Select | NP_001471.2:n.733-33C>G |