HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86575974G>T , CM000670.2:g.86575974G>T | GRCh38 |
NC_000008.10:g.87588202G>T , CM000670.1:g.87588202G>T | GRCh37 |
NC_000008.9:g.87657318G>T | NCBI36 |
NG_016980.1:g.172702C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000320005.6:c.2260C>A MANE Select | ENSP00000316605.5:p.Pro754Thr | |
ENST00000681546.1:n.2080C>A | ||
ENST00000681746.1:c.*671C>A | ENSP00000505959.1:n.*671C>A | |
ENST00000320005.5:c.2260C>A | ENSP00000316605.5:p.Pro754Thr | |
ENST00000517327.5:c.276+2715C>A | ENSP00000428329.1:n.276+2715C>A | |
NM_019098.4:c.2260C>A | NP_061971.3:p.Pro754Thr | |
XM_011517138.1:c.1846C>A | XP_011515440.1:p.Pro616Thr | |
XM_011517138.2:c.1846C>A | XP_011515440.1:p.Pro616Thr | |
NM_019098.5:c.2260C>A MANE Select | NP_061971.3:p.Pro754Thr |