HGVS | Genome Assembly |
---|---|
NC_000001.11:g.169525951C>G , CM000663.2:g.169525951C>G | GRCh38 |
NC_000001.10:g.169495189C>G , CM000663.1:g.169495189C>G | GRCh37 |
NC_000001.9:g.167761813C>G | NCBI36 |
NG_011806.1:g.65581G>C , LRG_553:g.65581G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000367797.9:c.5666G>C MANE Select | ENSP00000356771.3:p.Gly1889Ala | |
ENST00000367796.3:c.5681G>C | ENSP00000356770.3:p.Gly1894Ala | |
ENST00000367797.7:c.5666G>C | ENSP00000356771.3:p.Gly1889Ala | |
NM_000130.4:c.5666G>C , LRG_553t1:c.5666G>C | NP_000121.2:p.Gly1889Ala | |
XM_017000660.2:c.5255G>C | XP_016856149.1:p.Gly1752Ala | |
NM_000130.5:c.5666G>C MANE Select | NP_000121.2:p.Gly1889Ala |