HGVS | Genome Assembly |
---|---|
NC_000004.12:g.144559815C= , CM000666.2:g.144559815C= | GRCh38 |
NC_000004.11:g.145480967C= , CM000666.1:g.145480967C= | GRCh37 |
NC_000004.10:g.145700417C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000649263.1:c.328-143837G= | ENSP00000497507.1:n.328-143837G= | |
XR_939272.1:n.178+2169G= | ||
XR_939273.1:n.178+2169G= | ||
XR_939272.2:n.522+2169G= | ||
XR_939273.2:n.522+2169G= |