HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86579209C>A , CM000670.2:g.86579209C>A | GRCh38 |
NC_000008.10:g.87591437C>A , CM000670.1:g.87591437C>A | GRCh37 |
NC_000008.9:g.87660553C>A | NCBI36 |
NG_016980.1:g.169467G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000320005.6:c.1825G>T MANE Select | ENSP00000316605.5:p.Val609Leu | |
ENST00000681546.1:n.1645G>T | ||
ENST00000681746.1:c.*236G>T | ENSP00000505959.1:n.*236G>T | |
ENST00000320005.5:c.1825G>T | ENSP00000316605.5:p.Val609Leu | |
NM_019098.4:c.1825G>T | NP_061971.3:p.Val609Leu | |
XM_011517138.1:c.1411G>T | XP_011515440.1:p.Val471Leu | |
XM_011517138.2:c.1411G>T | XP_011515440.1:p.Val471Leu | |
NM_019098.5:c.1825G>T MANE Select | NP_061971.3:p.Val609Leu |