HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48411066T>A , CM000677.2:g.48411066T>A | GRCh38 |
NC_000015.9:g.48703263T>A , CM000677.1:g.48703263T>A | GRCh37 |
NC_000015.8:g.46490555T>A | NCBI36 |
NG_008805.2:g.239723A>T , LRG_778:g.239723A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.*1348A>T | ENSP00000453958.2:n.*1348A>T | |
ENST00000682158.1:n.1921A>T | ||
ENST00000682170.1:n.2721A>T | ||
ENST00000682767.1:n.1837A>T | ||
ENST00000316623.10:c.8540A>T MANE Select | ENSP00000325527.5:p.Asp2847Val | |
ENST00000316623.9:c.8540A>T | ENSP00000325527.5:p.Asp2847Val | |
ENST00000559133.5:c.3909A>T | ||
NM_000138.4:c.8540A>T , LRG_778t1:c.8540A>T | NP_000129.3:p.Asp2847Val | |
NM_000138.5:c.8540A>T MANE Select | NP_000129.3:p.Asp2847Val |