HGVS | Genome Assembly |
---|---|
NC_000017.11:g.74670881G>T , CM000679.2:g.74670881G>T | GRCh38 |
NC_000017.10:g.72667020G>T , CM000679.1:g.72667020G>T | GRCh37 |
NC_000017.9:g.70178615G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000340415.7:c.-706G>T | ENSP00000341354.3:n.-706G>T | |
XR_001753013.2:n.5739C>A |