Linked Data
MyVariant Identifiers:
chr20:g.34152692T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.35564776T>G , CM000682.2:g.35564776T>G | GRCh38 |
| NC_000020.10:g.34152692T>G , CM000682.1:g.34152692T>G | GRCh37 |
| NC_000020.9:g.33616106T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000674340.1:n.2116A>C | ||
| ENST00000674470.1:n.1443A>C | ||
| ENST00000611673.4:n.1137A>C | ||
| ENST00000613061.4:n.1487A>C | ||
| ENST00000615531.4:n.4652A>C | ||
| ENST00000616711.4:n.1801A>C | ||
| ENST00000621044.4:n.765A>C | ||
| NR_119376.1:n.4664A>C |