HGVS | Genome Assembly |
---|---|
NC_000001.11:g.169541770T>C , CM000663.2:g.169541770T>C | GRCh38 |
NC_000001.10:g.169511008T>C , CM000663.1:g.169511008T>C | GRCh37 |
NC_000001.9:g.167777632T>C | NCBI36 |
NG_011806.1:g.49762A>G , LRG_553:g.49762A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367797.9:c.3320A>G MANE Select | ENSP00000356771.3:p.Asp1107Gly | |
ENST00000367796.3:c.3335A>G | ENSP00000356770.3:p.Asp1112Gly | |
ENST00000367797.7:c.3320A>G | ENSP00000356771.3:p.Asp1107Gly | |
NM_000130.4:c.3320A>G , LRG_553t1:c.3320A>G | NP_000121.2:p.Asp1107Gly | |
XM_017000660.2:c.2909A>G | XP_016856149.1:p.Asp970Gly | |
NM_000130.5:c.3320A>G MANE Select | NP_000121.2:p.Asp1107Gly |