HGVS | Genome Assembly |
---|---|
NC_000017.11:g.44375707C>G , CM000679.2:g.44375707C>G | GRCh38 |
NC_000017.10:g.42453075C>G , CM000679.1:g.42453075C>G | GRCh37 |
NC_000017.9:g.39808601C>G | NCBI36 |
NG_008331.1:g.18799G>C , LRG_479:g.18799G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000262407.6:c.2611G>C MANE Select | ENSP00000262407.5:p.Gly871Arg | |
ENST00000648408.1:c.2042G>C | ||
ENST00000262407.5:c.2611G>C | ENSP00000262407.5:p.Gly871Arg | |
ENST00000587295.5:c.253+126G>C | ||
ENST00000592462.5:n.1406G>C | ||
NM_000419.3:c.2611G>C , LRG_479t1:c.2611G>C | NP_000410.2:p.Gly871Arg | |
XM_011524749.1:c.2611G>C | XP_011523051.1:p.Gly871Arg | |
XM_011524750.1:c.2611G>C | XP_011523052.1:p.Gly871Arg | |
NM_000419.4:c.2611G>C | NP_000410.2:p.Gly871Arg | |
NM_000419.5:c.2611G>C MANE Select | NP_000410.2:p.Gly871Arg |