Linked Data
MyVariant Identifiers:
chr20:g.34152698T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.35564782T>G , CM000682.2:g.35564782T>G | GRCh38 |
| NC_000020.10:g.34152698T>G , CM000682.1:g.34152698T>G | GRCh37 |
| NC_000020.9:g.33616112T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000674340.1:n.2110A>C | ||
| ENST00000674470.1:n.1437A>C | ||
| ENST00000611673.4:n.1131A>C | ||
| ENST00000613061.4:n.1481A>C | ||
| ENST00000615531.4:n.4646A>C | ||
| ENST00000616711.4:n.1795A>C | ||
| ENST00000621044.4:n.759A>C | ||
| NR_119376.1:n.4658A>C |