HGVS | Genome Assembly |
---|---|
NC_000016.10:g.73679692T= , CM000678.2:g.73679692T= | GRCh38 |
NC_000016.9:g.73713591T= , CM000678.1:g.73713591T= | GRCh37 |
NC_000016.8:g.72271092T= | NCBI36 |
NG_013211.2:g.217240A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000641018.1:n.649A= | ||
ENST00000641206.2:c.-1547+488A= | ENSP00000493252.1:n.-1547+488A= | |
ENST00000642085.1:n.163+488A= | ||
XR_933730.1:n.355+488A= | ||
XM_024450275.1:c.-494+488A= | XP_024306043.1:n.-494+488A= | |
NM_001386735.1:c.-1064+488A= | NP_001373664.1:n.-1064+488A= |