HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48411022G>A , CM000677.2:g.48411022G>A | GRCh38 |
NC_000015.9:g.48703219G>A , CM000677.1:g.48703219G>A | GRCh37 |
NC_000015.8:g.46490511G>A | NCBI36 |
NG_008805.2:g.239767C>T , LRG_778:g.239767C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.*1392C>T | ENSP00000453958.2:n.*1392C>T | |
ENST00000682158.1:n.1965C>T | ||
ENST00000682170.1:n.2765C>T | ||
ENST00000682767.1:n.1881C>T | ||
ENST00000316623.10:c.8584C>T MANE Select | ENSP00000325527.5:p.Leu2862= | |
ENST00000316623.9:c.8584C>T | ENSP00000325527.5:p.Leu2862= | |
ENST00000559133.5:c.3953C>T | ||
NM_000138.4:c.8584C>T , LRG_778t1:c.8584C>T | NP_000129.3:p.Leu2862= | |
NM_000138.5:c.8584C>T MANE Select | NP_000129.3:p.Leu2862= |