HGVS | Genome Assembly |
---|---|
NC_000005.10:g.145585786C>T , CM000667.2:g.145585786C>T | GRCh38 |
NC_000005.9:g.144965349C>T , CM000667.1:g.144965349C>T | GRCh37 |
NC_000005.8:g.144945542C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000510259.5:n.71-112471G>A | ||
XR_944308.1:n.662+179145G>A |