HGVS | Genome Assembly |
---|---|
NC_000006.12:g.42722289A>T , CM000668.2:g.42722289A>T | GRCh38 |
NC_000006.11:g.42690027A>T , CM000668.1:g.42690027A>T | GRCh37 |
NC_000006.10:g.42798005A>T | NCBI36 |
NG_009176.1:g.5332T>A | |
NG_009176.2:g.5332T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000230381.7:c.46T>A MANE Select | ENSP00000230381.5:p.Leu16Met | |
ENST00000230381.6:c.46T>A | ENSP00000230381.5:p.Leu16Met | |
NM_000322.4:c.46T>A | NP_000313.2:p.Leu16Met | |
XR_427834.2:n.701T>A | ||
XR_926295.1:n.701T>A | ||
XR_427834.4:n.751T>A | ||
XR_926295.3:n.751T>A | ||
NM_000322.5:c.46T>A MANE Select | NP_000313.2:p.Leu16Met |