HGVS | Genome Assembly |
---|---|
NC_000004.12:g.144559814A= , CM000666.2:g.144559814A= | GRCh38 |
NC_000004.11:g.145480966A= , CM000666.1:g.145480966A= | GRCh37 |
NC_000004.10:g.145700416A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000649263.1:c.328-143836T= | ENSP00000497507.1:n.328-143836T= | |
XR_939272.1:n.178+2170T= | ||
XR_939273.1:n.178+2170T= | ||
XR_939272.2:n.522+2170T= | ||
XR_939273.2:n.522+2170T= |