HGVS | Genome Assembly |
---|---|
NC_000017.11:g.14069513A= , CM000679.2:g.14069513A= | GRCh38 |
NC_000017.10:g.13972830A= , CM000679.1:g.13972830A= | GRCh37 |
NC_000017.9:g.13913555A= | NCBI36 |
NG_008034.1:g.5112A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261643.8:c.-93A= MANE Select | ENSP00000261643.3:n.-93A= | |
ENST00000664217.1:c.-93A= | ENSP00000499396.1:n.-93A= | |
ENST00000670279.1:c.-93A= | ENSP00000499450.1:n.-93A= | |
ENST00000429152.6:c.-93A= | ENSP00000397750.2:n.-93A= | |
NM_001303.3:c.-93A= | NP_001294.2:n.-93A= | |
XM_005256458.1:c.-93A= | XP_005256515.1:n.-93A= | |
XM_011523657.1:c.-93A= | XP_011521959.1:n.-93A= | |
XM_011523658.1:c.-544A= | XP_011521960.1:n.-544A= | |
XR_933974.1:n.11A= | ||
XR_933975.1:n.11A= | ||
NM_001303.4:c.-93A= MANE Select | NP_001294.2:n.-93A= |