HGVS | Genome Assembly |
---|---|
NC_000017.11:g.14208813A= , CM000679.2:g.14208813A= | GRCh38 |
NC_000017.10:g.14112130A= , CM000679.1:g.14112130A= | GRCh37 |
NC_000017.9:g.14052855A= | NCBI36 |
NG_008034.1:g.144412A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000664217.1:c.*281+34A= | ENSP00000499396.1:n.*281+34A= | |
ENST00000670279.1:c.929-696A= | ENSP00000499450.1:n.929-696A= | |
XR_933974.1:n.1032-696A= |