HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48410865T>C , CM000677.2:g.48410865T>C | GRCh38 |
NC_000015.9:g.48703062T>C , CM000677.1:g.48703062T>C | GRCh37 |
NC_000015.8:g.46490354T>C | NCBI36 |
NG_008805.2:g.239924A>G , LRG_778:g.239924A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.*1549A>G | ENSP00000453958.2:n.*1549A>G | |
ENST00000682158.1:n.2122A>G | ||
ENST00000682170.1:n.2922A>G | ||
ENST00000682767.1:n.2038A>G | ||
ENST00000316623.10:c.*125A>G MANE Select | ENSP00000325527.5:n.*125A>G | |
ENST00000316623.9:c.*125A>G | ENSP00000325527.5:n.*125A>G | |
ENST00000559133.5:c.4110A>G | ||
NM_000138.4:c.*125A>G , LRG_778t1:c.*125A>G | NP_000129.3:n.*125A>G | |
NM_000138.5:c.*125A>G MANE Select | NP_000129.3:n.*125A>G |