Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52520007A>C , CM000674.2:g.52520007A>C | GRCh38 |
| NC_000012.11:g.52913791A>C , CM000674.1:g.52913791A>C | GRCh37 |
| NC_000012.10:g.51200058A>C | NCBI36 |
| NG_008297.1:g.5453T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252242.9:c.290T>G MANE Select | ENSP00000252242.4:p.Phe97Cys | |
| ENST00000252242.8:c.290T>G | ENSP00000252242.4:p.Phe97Cys | |
| ENST00000546577.1:c.290T>G | ENSP00000449651.1:p.Phe97Cys | |
| ENST00000549420.1:c.44-84T>G | ENSP00000447209.1:n.44-84T>G | |
| ENST00000551275.1:c.185T>G | ENSP00000448041.1:p.Phe62Cys | |
| ENST00000552629.5:n.388T>G | ||
| NM_000424.3:c.290T>G | NP_000415.2:p.Phe97Cys | |
| NM_000424.4:c.290T>G MANE Select | NP_000415.2:p.Phe97Cys |