HGVS | Genome Assembly |
---|---|
NC_000013.11:g.27924284G>C , CM000675.2:g.27924284G>C | GRCh38 |
NC_000013.10:g.28498421G>C , CM000675.1:g.28498421G>C | GRCh37 |
NC_000013.9:g.27396421G>C | NCBI36 |
NG_008183.1:g.9254G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381033.5:c.435G>C MANE Select | ENSP00000370421.4:p.Glu145Asp | |
ENST00000381033.4:c.435G>C | ENSP00000370421.4:p.Glu145Asp | |
NM_000209.3:c.435G>C | NP_000200.1:p.Glu145Asp | |
XR_941578.1:n.3562G>C | ||
XR_941579.1:n.2161G>C | ||
XR_941580.1:n.1077G>C | ||
XR_941578.2:n.3574G>C | ||
XR_941580.2:n.1089G>C | ||
NM_000209.4:c.435G>C MANE Select | NP_000200.1:p.Glu145Asp |