HGVS | Genome Assembly |
---|---|
NC_000020.11:g.33408801C>A , CM000682.2:g.33408801C>A | GRCh38 |
NC_000020.10:g.31996607C>A , CM000682.1:g.31996607C>A | GRCh37 |
NC_000020.9:g.31460268C>A | NCBI36 |
NG_011622.1:g.40092G>T , LRG_332:g.40092G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000217381.3:c.1325G>T MANE Select | ENSP00000217381.2:p.Arg442Leu | |
ENST00000217381.2:c.1325G>T | ENSP00000217381.2:p.Arg442Leu | |
NM_003098.2:c.1325G>T , LRG_332t1:c.1325G>T | NP_003089.1:p.Arg442Leu | |
XM_005260517.1:c.1325G>T | XP_005260574.1:p.Arg442Leu | |
XM_011529007.1:c.1357G>T | XP_011527309.1:p.Glu453Ter | |
XM_011529008.1:c.1357G>T | XP_011527310.1:p.Glu453Ter | |
XR_936612.1:n.1361G>T | ||
XM_024451971.1:c.998G>T | XP_024307739.1:p.Arg333Leu | |
NM_003098.3:c.1325G>T MANE Select | NP_003089.1:p.Arg442Leu |