Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.38144331A>C , CM000670.2:g.38144331A>C | GRCh38 |
| NC_000008.10:g.38001849A>C , CM000670.1:g.38001849A>C | GRCh37 |
| NC_000008.9:g.38121006A>C | NCBI36 |
| NG_011827.1:g.11752T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000276449.9:c.800T>G MANE Select | ENSP00000276449.3:p.Phe267Cys | |
| ENST00000276449.8:c.800T>G | ENSP00000276449.3:p.Phe267Cys | |
| ENST00000520114.1:n.2769T>G | ||
| ENST00000522050.1:c.642T>G | ||
| NM_000349.2:c.800T>G | NP_000340.2:p.Phe267Cys | |
| XM_006716392.1:c.706T>G | XP_006716455.1:p.Leu236Val | |
| NM_000349.3:c.800T>G MANE Select | NP_000340.2:p.Phe267Cys |