Linked Data
MyVariant Identifiers:
chr10:g.79540645T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.77780887T>G , CM000672.2:g.77780887T>G | GRCh38 |
| NC_000010.10:g.79540645T>G , CM000672.1:g.79540645T>G | GRCh37 |
| NC_000010.9:g.79210651T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000439688.1:n.990A>C |