Linked Data
MyVariant Identifiers:
chr10:g.93349713C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.91589956C>T , CM000672.2:g.91589956C>T | GRCh38 |
| NC_000010.10:g.93349713C>T , CM000672.1:g.93349713C>T | GRCh37 |
| NC_000010.9:g.93339693C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_024467.1:n.110+21395G>A |