Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3225595T>G , CM000668.2:g.3225595T>G | GRCh38 |
| NC_000006.11:g.3225829T>G , CM000668.1:g.3225829T>G | GRCh37 |
| NC_000006.10:g.3170828T>G | NCBI36 |
| NG_016715.1:g.7140A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259818.8:c.494A>C MANE Select | ENSP00000259818.6:p.Asn165Thr | |
| ENST00000680070.1:n.1424A>C | ||
| ENST00000681707.1:n.1321A>C | ||
| ENST00000681757.1:n.799A>C | ||
| ENST00000259818.7:c.494A>C | ENSP00000259818.6:p.Asn165Thr | |
| ENST00000473006.1:n.611A>C | ||
| NM_178012.4:c.494A>C | NP_821080.1:p.Asn165Thr | |
| XM_011514571.1:c.278A>C | XP_011512873.1:p.Asn93Thr | |
| NM_178012.5:c.494A>C MANE Select | NP_821080.1:p.Asn165Thr |