Linked Data
MyVariant Identifiers:
chr10:g.94179012G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.92419255G>T , CM000672.2:g.92419255G>T | GRCh38 |
| NC_000010.10:g.94179012G>T , CM000672.1:g.94179012G>T | GRCh37 |
| NC_000010.9:g.94168992G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000430958.1:n.589G>T | ||
| NR_038243.2:n.595G>T |