HGVS | Genome Assembly |
---|---|
NC_000003.12:g.14129412T= , CM000665.2:g.14129412T= | GRCh38 |
NC_000003.11:g.14170912T= , CM000665.1:g.14170912T= | GRCh37 |
NC_000003.10:g.14145913T= | NCBI36 |
NG_008975.1:g.9473T= , LRG_435:g.9473T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000432444.2:c.*43T= | ENSP00000395617.1:n.*43T= | |
ENST00000306077.5:c.13T= MANE Select | ENSP00000303992.5:p.Tyr5= | |
ENST00000306077.4:c.13T= | ENSP00000303992.4:p.Tyr5= | |
ENST00000432444.1:c.*43T= | ENSP00000395617.1:n.*43T= | |
NM_024334.2:c.13T= , LRG_435t1:c.13T= | NP_077310.1:p.Tyr5= | |
XM_011534109.1:c.-93T= | XP_011532411.1:n.-93T= | |
XM_017007176.2:c.-93T= | XP_016862665.1:n.-93T= | |
NM_024334.3:c.13T= MANE Select | NP_077310.1:p.Tyr5= |