HGVS | Genome Assembly |
---|---|
NC_000017.11:g.7668244C= , CM000679.2:g.7668244C= | GRCh38 |
NC_000017.10:g.7571562C= , CM000679.1:g.7571562C= | GRCh37 |
NC_000017.9:g.7512287C= | NCBI36 |
NG_017013.2:g.24307G= , LRG_321:g.24307G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000359597.8:c.994-2000G= | ENSP00000352610.4:n.994-2000G= | |
ENST00000413465.6:c.782+5937G= | ENSP00000410739.2:n.782+5937G= | |
ENST00000635293.1:c.984-819G= | ENSP00000488924.1:n.984-819G= |