HGVS | Genome Assembly |
---|---|
NC_000004.12:g.67932052C= , CM000666.2:g.67932052C= | GRCh38 |
NC_000004.11:g.68797770C= , CM000666.1:g.68797770C= | GRCh37 |
NC_000004.10:g.68480365C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000508048.6:c.261G= MANE Select | ENSP00000426911.2:p.Glu87= | |
ENST00000334830.11:c.270G= | ENSP00000334611.7:p.Glu90= | |
ENST00000396188.3:c.261G= | ENSP00000379491.3:p.Glu87= | |
ENST00000508048.5:c.261G= | ENSP00000426911.2:p.Glu87= | |
ENST00000513536.5:c.201G= | ENSP00000427621.1:p.Glu67= | |
NM_001114387.1:c.261G= | NP_001107859.1:p.Glu87= | |
NM_182606.3:c.270G= | NP_872412.3:p.Glu90= | |
NM_001114387.2:c.261G= MANE Select | NP_001107859.1:p.Glu87= | |
NM_182606.4:c.270G= | NP_872412.3:p.Glu90= |