HGVS | Genome Assembly |
---|---|
NC_000010.11:g.80275062G>C , CM000672.2:g.80275062G>C | GRCh38 |
NC_000010.10:g.82034818G>C , CM000672.1:g.82034818G>C | GRCh37 |
NC_000010.9:g.82024798G>C | NCBI36 |
NG_008083.1:g.19617C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372213.8:c.906C>G MANE Select | ENSP00000361287.3:p.Ala302= | |
ENST00000372213.7:c.906C>G | ENSP00000361287.3:p.Ala302= | |
ENST00000480845.1:n.138C>G | ||
ENST00000485270.5:n.418C>G | ||
NM_000429.2:c.906C>G | NP_000420.1:p.Ala302= | |
XM_005269842.3:c.906C>G | XP_005269899.1:p.Ala302= | |
XM_005269843.3:c.783C>G | XP_005269900.1:p.Ala261= | |
NM_000429.3:c.906C>G MANE Select | NP_000420.1:p.Ala302= |