Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48875912C>G , CM000681.2:g.48875912C>G | GRCh38 |
| NC_000019.9:g.49379169C>G , CM000681.1:g.49379169C>G | GRCh37 |
| NC_000019.8:g.54070981C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000600406.2:c.*819C>G | ENSP00000469239.2:n.*819C>G | |
| ENST00000704026.1:c.1679C>G | ENSP00000515636.1:p.Thr560Arg | |
| ENST00000704027.1:c.2012C>G | ENSP00000515637.1:p.Thr671Arg | |
| ENST00000200453.6:c.1964C>G MANE Select | ENSP00000200453.4:p.Thr655Arg | |
| ENST00000200453.5:c.1964C>G | ENSP00000200453.4:p.Thr655Arg | |
| ENST00000600406.1:c.1595C>G | ||
| NM_014330.3:c.1964C>G | NP_055145.3:p.Thr655Arg | |
| NM_014330.5:c.1964C>G MANE Select | NP_055145.3:p.Thr655Arg |