Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154074G>C , CM000681.2:g.55154074G>C | GRCh38 |
| NC_000019.9:g.55665442G>C , CM000681.1:g.55665442G>C | GRCh37 |
| NC_000019.8:g.60357254G>C | NCBI36 |
| NG_007866.2:g.8659C>G , LRG_432:g.8659C>G | |
| NG_011829.2:g.165C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.505C>G MANE Select | ENSP00000341838.5:p.Leu169Val | |
| ENST00000665070.1:c.538C>G | ENSP00000499482.1:p.Leu180Val | |
| ENST00000344887.9:c.505C>G | ENSP00000341838.5:p.Leu169Val | |
| ENST00000585806.5:n.504C>G | ||
| ENST00000588882.1:c.430C>G | ENSP00000466729.1:p.Leu144Val | |
| ENST00000589864.1:n.333C>G | ||
| NM_000363.4:c.505C>G , LRG_432t1:c.505C>G | NP_000354.4:p.Leu169Val | |
| NM_000363.5:c.505C>G MANE Select | NP_000354.4:p.Leu169Val |