HGVS | Genome Assembly |
---|---|
NC_000006.12:g.77463564T>C , CM000668.2:g.77463564T>C | GRCh38 |
NC_000006.11:g.78173281T>C , CM000668.1:g.78173281T>C | GRCh37 |
NC_000006.10:g.78230000T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NM_000863.2:c.-161A>G | NP_000854.1:n.-161A>G | |
XR_942706.1:n.545-10962T>C | ||
XR_942707.1:n.545-10962T>C | ||
XR_942708.1:n.545-10962T>C | ||
XR_942709.1:n.545-10962T>C | ||
XR_942708.2:n.545-10962T>C |