HGVS | Genome Assembly |
---|---|
NC_000015.10:g.64162877T>A , CM000677.2:g.64162877T>A | GRCh38 |
NC_000015.9:g.64455076T>A , CM000677.1:g.64455076T>A | GRCh37 |
NC_000015.8:g.62242129T>A | NCBI36 |
NG_012979.1:g.5279A>T , LRG_10:g.5279A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000300026.4:c.110A>T MANE Select | ENSP00000300026.4:p.Lys37Met | |
ENST00000561048.2:n.143A>T | ||
ENST00000680158.1:c.110A>T | ENSP00000504873.1:p.Lys37Met | |
ENST00000681397.1:c.110A>T | ENSP00000506584.1:p.Lys37Met | |
ENST00000681658.1:c.30+80A>T | ENSP00000505431.1:n.30+80A>T | |
ENST00000300026.3:c.110A>T | ENSP00000300026.3:p.Lys37Met | |
ENST00000558492.1:n.130A>T | ||
ENST00000561048.1:n.145A>T | ||
NM_000942.4:c.110A>T , LRG_10t1:c.110A>T | NP_000933.1:p.Lys37Met | |
NM_000942.5:c.110A>T MANE Select | NP_000933.1:p.Lys37Met |