Linked Data
MyVariant Identifiers:
chr20:g.34152782C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.35564866C>A , CM000682.2:g.35564866C>A | GRCh38 |
| NC_000020.10:g.34152782C>A , CM000682.1:g.34152782C>A | GRCh37 |
| NC_000020.9:g.33616196C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000674340.1:n.2026G>T | ||
| ENST00000674470.1:n.1353G>T | ||
| ENST00000611673.4:n.1047G>T | ||
| ENST00000613061.4:n.1397G>T | ||
| ENST00000615531.4:n.4562G>T | ||
| ENST00000616711.4:n.1711G>T | ||
| ENST00000621044.4:n.675G>T | ||
| NR_119376.1:n.4574G>T |