HGVS | Genome Assembly |
---|---|
NC_000017.11:g.14208736T>G , CM000679.2:g.14208736T>G | GRCh38 |
NC_000017.10:g.14112053T>G , CM000679.1:g.14112053T>G | GRCh37 |
NC_000017.9:g.14052778T>G | NCBI36 |
NG_008034.1:g.144335T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000664217.1:c.*238T>G | ENSP00000499396.1:n.*238T>G | |
ENST00000670279.1:c.929-773T>G | ENSP00000499450.1:n.929-773T>G | |
XR_933974.1:n.1032-773T>G |