HGVS | Genome Assembly |
---|---|
NC_000003.12:g.14129551T>G , CM000665.2:g.14129551T>G | GRCh38 |
NC_000003.11:g.14171051T>G , CM000665.1:g.14171051T>G | GRCh37 |
NC_000003.10:g.14146052T>G | NCBI36 |
NG_008975.1:g.9612T>G , LRG_435:g.9612T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000432444.2:c.*182T>G | ENSP00000395617.1:n.*182T>G | |
ENST00000306077.5:c.152T>G MANE Select | ENSP00000303992.5:p.Phe51Cys | |
ENST00000306077.4:c.152T>G | ENSP00000303992.4:p.Phe51Cys | |
ENST00000432444.1:c.*182T>G | ENSP00000395617.1:n.*182T>G | |
NM_024334.2:c.152T>G , LRG_435t1:c.152T>G | NP_077310.1:p.Phe51Cys | |
XM_011534109.1:c.47T>G | XP_011532411.1:p.Phe16Cys | |
XM_017007176.2:c.47T>G | XP_016862665.1:p.Phe16Cys | |
NM_024334.3:c.152T>G MANE Select | NP_077310.1:p.Phe51Cys |