Linked Data
MyVariant Identifiers:
chr17:g.69108837C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.71112696C>T , CM000679.2:g.71112696C>T | GRCh38 |
| NC_000017.10:g.69108837C>T , CM000679.1:g.69108837C>T | GRCh37 |
| NC_000017.9:g.66620432C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_104152.1:n.218-13078G>A |