HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86671008T>A , CM000670.2:g.86671008T>A | GRCh38 |
NC_000008.10:g.87683236T>A , CM000670.1:g.87683236T>A | GRCh37 |
NC_000008.9:g.87752352T>A | NCBI36 |
NG_016980.1:g.77668A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320005.6:c.429A>T MANE Select | ENSP00000316605.5:p.Thr143= | |
ENST00000680314.1:n.190A>T | ||
ENST00000681746.1:c.429A>T | ENSP00000505959.1:p.Thr143= | |
ENST00000320005.5:c.429A>T | ENSP00000316605.5:p.Thr143= | |
NM_019098.4:c.429A>T | NP_061971.3:p.Thr143= | |
XM_011517138.1:c.15A>T | XP_011515440.1:p.Thr5= | |
XM_011517138.2:c.15A>T | XP_011515440.1:p.Thr5= | |
NM_019098.5:c.429A>T MANE Select | NP_061971.3:p.Thr143= |