HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31524583G>T , CM000680.2:g.31524583G>T | GRCh38 |
NC_000018.9:g.29104546G>T , CM000680.1:g.29104546G>T | GRCh37 |
NC_000018.8:g.27358544G>T | NCBI36 |
NG_007072.3:g.31342G>T , LRG_397:g.31342G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000682087.2:n.657G>T | ||
ENST00000683614.2:n.657G>T | ||
ENST00000682087.1:c.657G>T | ||
ENST00000683614.1:c.657G>T | ||
ENST00000261590.13:c.826G>T MANE Select | ENSP00000261590.8:p.Val276Leu | |
ENST00000261590.12:c.826G>T | ENSP00000261590.8:p.Val276Leu | |
NM_001943.3:c.826G>T , LRG_397t1:c.826G>T | NP_001934.2:p.Val276Leu | |
NM_001943.4:c.826G>T | NP_001934.2:p.Val276Leu | |
XM_024451095.1:c.292G>T | XP_024306863.1:p.Val98Leu | |
NM_001943.5:c.826G>T MANE Select | NP_001934.2:p.Val276Leu |