HGVS | Genome Assembly |
---|---|
NC_000017.11:g.14208760C= , CM000679.2:g.14208760C= | GRCh38 |
NC_000017.10:g.14112077C= , CM000679.1:g.14112077C= | GRCh37 |
NC_000017.9:g.14052802C= | NCBI36 |
NG_008034.1:g.144359C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000664217.1:c.*262C= | ENSP00000499396.1:n.*262C= | |
ENST00000670279.1:c.929-749C= | ENSP00000499450.1:n.929-749C= | |
XR_933974.1:n.1032-749C= |