HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186205232G>A , CM000666.2:g.186205232G>A | GRCh38 |
NC_000004.11:g.187126386G>A , CM000666.1:g.187126386G>A | GRCh37 |
NC_000004.10:g.187363380G>A | NCBI36 |
NG_007965.1:g.18713G>A | |
NG_012095.2:g.1254G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378802.5:c.1020G>A MANE Select | ENSP00000368079.4:p.Trp340Ter | |
ENST00000378802.4:c.1020G>A | ENSP00000368079.4:p.Trp340Ter | |
ENST00000502665.1:n.255G>A | ||
ENST00000507209.5:n.5718G>A | ||
ENST00000513354.5:n.110G>A | ||
NM_207352.3:c.1020G>A | NP_997235.3:p.Trp340Ter | |
XM_005262935.2:c.1020G>A | XP_005262992.1:p.Trp340Ter | |
XM_006714184.2:c.624G>A | XP_006714247.1:p.Trp208Ter | |
XM_005262935.4:c.1020G>A | XP_005262992.1:p.Trp340Ter | |
XM_017008037.1:c.624G>A | XP_016863526.1:p.Trp208Ter | |
NM_207352.4:c.1020G>A MANE Select | NP_997235.3:p.Trp340Ter |