HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48411040C>G , CM000677.2:g.48411040C>G | GRCh38 |
NC_000015.9:g.48703237C>G , CM000677.1:g.48703237C>G | GRCh37 |
NC_000015.8:g.46490529C>G | NCBI36 |
NG_008805.2:g.239749G>C , LRG_778:g.239749G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.*1374G>C | ENSP00000453958.2:n.*1374G>C | |
ENST00000682158.1:n.1947G>C | ||
ENST00000682170.1:n.2747G>C | ||
ENST00000682767.1:n.1863G>C | ||
ENST00000316623.10:c.8566G>C MANE Select | ENSP00000325527.5:p.Gly2856Arg | |
ENST00000316623.9:c.8566G>C | ENSP00000325527.5:p.Gly2856Arg | |
ENST00000559133.5:c.3935G>C | ||
NM_000138.4:c.8566G>C , LRG_778t1:c.8566G>C | NP_000129.3:p.Gly2856Arg | |
NM_000138.5:c.8566G>C MANE Select | NP_000129.3:p.Gly2856Arg |