HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110812673A>G , CM000672.2:g.110812673A>G | GRCh38 |
NC_000010.10:g.112572431A>G , CM000672.1:g.112572431A>G | GRCh37 |
NC_000010.9:g.112562421A>G | NCBI36 |
NG_021177.1:g.173277A>G , LRG_382:g.173277A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369519.4:c.2276A>G MANE Select | ENSP00000358532.3:p.Tyr759Cys | |
ENST00000369519.3:c.2276A>G | ENSP00000358532.3:p.Tyr759Cys | |
NM_001134363.2:c.2276A>G | NP_001127835.2:p.Tyr759Cys | |
XM_011539697.1:c.1892A>G | XP_011537999.1:p.Tyr631Cys | |
XM_017016103.2:c.2111A>G | XP_016871592.1:p.Tyr704Cys | |
XM_017016104.2:c.1892A>G | XP_016871593.1:p.Tyr631Cys | |
NM_001134363.3:c.2276A>G MANE Select | NP_001127835.2:p.Tyr759Cys |