HGVS | Genome Assembly |
---|---|
NC_000008.11:g.27572989A>T , CM000670.2:g.27572989A>T | GRCh38 |
NC_000008.10:g.27430506A>T , CM000670.1:g.27430506A>T | GRCh37 |
NC_000008.9:g.27486423A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000454030.1:n.198-4622A>T (GULOP) | ||
XR_001745491.1:n.1648-19344A>T (EPHX2) |