HGVS | Genome Assembly |
---|---|
NC_000017.11:g.14069508C= , CM000679.2:g.14069508C= | GRCh38 |
NC_000017.10:g.13972825C= , CM000679.1:g.13972825C= | GRCh37 |
NC_000017.9:g.13913550C= | NCBI36 |
NG_008034.1:g.5107C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261643.8:c.-98C= MANE Select | ENSP00000261643.3:n.-98C= | |
ENST00000664217.1:c.-98C= | ENSP00000499396.1:n.-98C= | |
ENST00000670279.1:c.-98C= | ENSP00000499450.1:n.-98C= | |
ENST00000429152.6:c.-98C= | ENSP00000397750.2:n.-98C= | |
NM_001303.3:c.-98C= | NP_001294.2:n.-98C= | |
XM_005256458.1:c.-98C= | XP_005256515.1:n.-98C= | |
XM_011523657.1:c.-98C= | XP_011521959.1:n.-98C= | |
XM_011523658.1:c.-549C= | XP_011521960.1:n.-549C= | |
XR_933974.1:n.6C= | ||
XR_933975.1:n.6C= | ||
NM_001303.4:c.-98C= MANE Select | NP_001294.2:n.-98C= |