Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8075711A>G , CM000679.2:g.8075711A>G | GRCh38 |
| NC_000017.10:g.7979029A>G , CM000679.1:g.7979029A>G | GRCh37 |
| NC_000017.9:g.7919754A>G | NCBI36 |
| NG_007099.1:g.16993T>C | |
| NG_007099.2:g.17006T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647874.1:c.1538T>C MANE Select | ENSP00000497784.1:p.Val513Ala | |
| ENST00000649809.1:c.602T>C | ENSP00000496845.1:p.Val201Ala | |
| ENST00000319144.4:c.1538T>C | ENSP00000315167.4:p.Val513Ala | |
| ENST00000577351.5:n.479+464T>C | ||
| NM_001139.2:c.1538T>C | NP_001130.1:p.Val513Ala | |
| NM_001139.3:c.1538T>C MANE Select | NP_001130.1:p.Val513Ala |