HGVS | Genome Assembly |
---|---|
NC_000013.11:g.39329162T>C , CM000675.2:g.39329162T>C | GRCh38 |
NC_000013.10:g.39903299T>C , CM000675.1:g.39903299T>C | GRCh37 |
NC_000013.9:g.38801299T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648377.1:c.*82+14692A>G | ENSP00000496801.1:n.*82+14692A>G | |
XR_001749845.1:n.1449+7109A>G |