Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1985874G>C , CM000678.2:g.1985874G>C | GRCh38 |
| NC_000016.9:g.2035875G>C , CM000678.1:g.2035875G>C | GRCh37 |
| NC_000016.8:g.1975876G>C | NCBI36 |
| NG_016288.1:g.6726G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000567719.2:c.239G>C | ENSP00000455885.1:p.Arg80Thr | |
| ENST00000248114.7:c.464G>C MANE Select | ENSP00000248114.6:p.Arg155Thr | |
| ENST00000248114.6:c.464G>C | ENSP00000248114.6:p.Arg155Thr | |
| ENST00000565658.1:n.621G>C | ||
| ENST00000567719.1:c.239G>C | ENSP00000455885.1:p.Arg80Thr | |
| ENST00000569451.1:c.267G>C | ENSP00000456432.1:p.Gln89His | |
| NM_005262.2:c.464G>C | NP_005253.3:p.Arg155Thr | |
| NM_005262.3:c.464G>C MANE Select | NP_005253.3:p.Arg155Thr |