HGVS | Genome Assembly |
---|---|
NC_000017.11:g.14208782G>T , CM000679.2:g.14208782G>T | GRCh38 |
NC_000017.10:g.14112099G>T , CM000679.1:g.14112099G>T | GRCh37 |
NC_000017.9:g.14052824G>T | NCBI36 |
NG_008034.1:g.144381G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000664217.1:c.*281+3G>T | ENSP00000499396.1:n.*281+3G>T | |
ENST00000670279.1:c.929-727G>T | ENSP00000499450.1:n.929-727G>T | |
XR_933974.1:n.1032-727G>T |