HGVS | Genome Assembly |
---|---|
NC_000005.10:g.155967329A>C , CM000667.2:g.155967329A>C | GRCh38 |
NC_000005.9:g.155394339A>C , CM000667.1:g.155394339A>C | GRCh37 |
NC_000005.8:g.155326917A>C | NCBI36 |
NG_008693.2:g.101986A>C , LRG_205:g.101986A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000517913.5:c.-282+96905A>C | ENSP00000429378.1:n.-282+96905A>C | |
XM_017009723.2:c.-208+96905A>C | XP_016865212.1:n.-208+96905A>C | |
XM_017009724.1:c.-207-156527A>C | XP_016865213.1:n.-207-156527A>C |