Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154085T>C , CM000681.2:g.55154085T>C | GRCh38 |
| NC_000019.9:g.55665453T>C , CM000681.1:g.55665453T>C | GRCh37 |
| NC_000019.8:g.60357265T>C | NCBI36 |
| NG_007866.2:g.8648A>G , LRG_432:g.8648A>G | |
| NG_011829.2:g.154A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.494A>G MANE Select | ENSP00000341838.5:p.Glu165Gly | |
| ENST00000665070.1:c.527A>G | ENSP00000499482.1:p.Glu176Gly | |
| ENST00000344887.9:c.494A>G | ENSP00000341838.5:p.Glu165Gly | |
| ENST00000585806.5:n.493A>G | ||
| ENST00000588882.1:c.419A>G | ENSP00000466729.1:p.Glu140Gly | |
| ENST00000589864.1:n.322A>G | ||
| NM_000363.4:c.494A>G , LRG_432t1:c.494A>G | NP_000354.4:p.Glu165Gly | |
| NM_000363.5:c.494A>G MANE Select | NP_000354.4:p.Glu165Gly |