Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10644908T>G , CM000682.2:g.10644908T>G | GRCh38 |
| NC_000020.10:g.10625556T>G , CM000682.1:g.10625556T>G | GRCh37 |
| NC_000020.9:g.10573556T>G | NCBI36 |
| NG_007496.1:g.34139A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.2299A>C MANE Select | ENSP00000254958.4:p.Thr767Pro | |
| ENST00000617965.2:n.2888A>C | ||
| ENST00000254958.9:c.2299A>C | ENSP00000254958.4:p.Thr767Pro | |
| ENST00000423891.6:n.2165A>C | ||
| ENST00000488480.2:n.696A>C | ||
| NM_000214.2:c.2299A>C | NP_000205.1:p.Thr767Pro | |
| NM_000214.3:c.2299A>C MANE Select | NP_000205.1:p.Thr767Pro |