HGVS | Genome Assembly |
---|---|
NC_000006.12:g.77463665A>T , CM000668.2:g.77463665A>T | GRCh38 |
NC_000006.11:g.78173382A>T , CM000668.1:g.78173382A>T | GRCh37 |
NC_000006.10:g.78230101A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NM_000863.2:c.-262T>A | NP_000854.1:n.-262T>A | |
XR_942706.1:n.545-10861A>T | ||
XR_942707.1:n.545-10861A>T | ||
XR_942708.1:n.545-10861A>T | ||
XR_942709.1:n.545-10861A>T | ||
XR_942708.2:n.545-10861A>T |