Linked Data
MyVariant Identifiers:
chr20:g.34152697C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.35564781C>T , CM000682.2:g.35564781C>T | GRCh38 |
| NC_000020.10:g.34152697C>T , CM000682.1:g.34152697C>T | GRCh37 |
| NC_000020.9:g.33616111C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000674340.1:n.2111G>A | ||
| ENST00000674470.1:n.1438G>A | ||
| ENST00000611673.4:n.1132G>A | ||
| ENST00000613061.4:n.1482G>A | ||
| ENST00000615531.4:n.4647G>A | ||
| ENST00000616711.4:n.1796G>A | ||
| ENST00000621044.4:n.760G>A | ||
| NR_119376.1:n.4659G>A |