HGVS | Genome Assembly |
---|---|
NC_000002.12:g.113062207T>A , CM000664.2:g.113062207T>A | GRCh38 |
NC_000002.11:g.113819784T>A , CM000664.1:g.113819784T>A | GRCh37 |
NC_000002.10:g.113536255T>A | NCBI36 |
NG_031864.1:g.8570T>A , LRG_730:g.8570T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000437409.2:c.199T>A | ENSP00000409262.2:p.Cys67Ser | |
ENST00000393200.7:c.199T>A MANE Select | ENSP00000376896.2:p.Cys67Ser | |
ENST00000346807.7:c.199T>A | ENSP00000259212.3:p.Cys67Ser | |
ENST00000393200.6:c.199T>A | ENSP00000376896.2:p.Cys67Ser | |
ENST00000437409.1:c.199T>A | ENSP00000409262.1:p.Cys67Ser | |
NM_012275.2:c.199T>A , LRG_730t2:c.199T>A | NP_036407.1:p.Cys67Ser | |
NM_173170.1:c.199T>A , LRG_730t1:c.199T>A | NP_775262.1:p.Cys67Ser | |
NM_012275.3:c.199T>A MANE Select | NP_036407.1:p.Cys67Ser |