Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.65077600C>G , CM000677.2:g.65077600C>G | GRCh38 |
| NC_000015.9:g.65369938C>G , CM000677.1:g.65369938C>G | GRCh37 |
| NC_000015.8:g.63156991C>G | NCBI36 |
| NG_021411.1:g.5785C>G , LRG_682:g.5785C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432196.5:c.785C>G MANE Select | ENSP00000388723.2:p.Ala262Gly | |
| ENST00000432196.3:c.785C>G | ENSP00000388723.2:p.Ala262Gly | |
| NM_001101362.2:c.785C>G , LRG_682t1:c.785C>G | NP_001094832.1:p.Ala262Gly | |
| NM_001101362.3:c.785C>G MANE Select | NP_001094832.1:p.Ala262Gly |