HGVS | Genome Assembly |
---|---|
NC_000002.12:g.113062470G= , CM000664.2:g.113062470G= | GRCh38 |
NC_000002.11:g.113820047G= , CM000664.1:g.113820047G= | GRCh37 |
NC_000002.10:g.113536518G= | NCBI36 |
NG_031864.1:g.8833G= , LRG_730:g.8833G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000437409.2:c.261G= | ENSP00000409262.2:p.Glu87= | |
ENST00000393200.7:c.261G= MANE Select | ENSP00000376896.2:p.Glu87= | |
ENST00000346807.7:c.261G= | ENSP00000259212.3:p.Glu87= | |
ENST00000393200.6:c.261G= | ENSP00000376896.2:p.Glu87= | |
ENST00000437409.1:c.261G= | ENSP00000409262.1:p.Glu87= | |
NM_012275.2:c.261G= , LRG_730t2:c.261G= | NP_036407.1:p.Glu87= | |
NM_173170.1:c.261G= , LRG_730t1:c.261G= | NP_775262.1:p.Glu87= | |
NM_012275.3:c.261G= MANE Select | NP_036407.1:p.Glu87= |