HGVS | Genome Assembly |
---|---|
NC_000003.12:g.180659477T>G , CM000665.2:g.180659477T>G | GRCh38 |
NC_000003.11:g.180377265T>G , CM000665.1:g.180377265T>G | GRCh37 |
NC_000003.10:g.181859959T>G | NCBI36 |
NG_029581.1:g.25019A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000476379.6:c.713A>C MANE Select | ENSP00000417960.2:p.Asp238Ala | |
ENST00000650641.1:n.792A>C | ||
ENST00000650889.1:n.885A>C | ||
ENST00000651046.1:c.713A>C | ENSP00000499175.1:p.Asp238Ala | |
ENST00000651818.1:n.855A>C | ||
ENST00000652024.1:n.804A>C | ||
ENST00000652408.1:n.850A>C | ||
ENST00000442201.6:c.713A>C | ENSP00000405708.2:p.Asp238Ala | |
ENST00000476379.5:c.713A>C | ENSP00000417960.1:p.Asp238Ala | |
NM_181426.1:c.713A>C | NP_852091.1:p.Asp238Ala | |
NM_181426.2:c.713A>C MANE Select | NP_852091.1:p.Asp238Ala |