Linked Data
MyVariant Identifiers:
chr20:g.34152691T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.35564775T>C , CM000682.2:g.35564775T>C | GRCh38 |
| NC_000020.10:g.34152691T>C , CM000682.1:g.34152691T>C | GRCh37 |
| NC_000020.9:g.33616105T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000674340.1:n.2117A>G | ||
| ENST00000674470.1:n.1444A>G | ||
| ENST00000611673.4:n.1138A>G | ||
| ENST00000613061.4:n.1488A>G | ||
| ENST00000615531.4:n.4653A>G | ||
| ENST00000616711.4:n.1802A>G | ||
| ENST00000621044.4:n.766A>G | ||
| NR_119376.1:n.4665A>G |