HGVS | Genome Assembly |
---|---|
NC_000003.12:g.14141614G= , CM000665.2:g.14141614G= | GRCh38 |
NC_000003.11:g.14183114G= , CM000665.1:g.14183114G= | GRCh37 |
NC_000003.10:g.14158115G= | NCBI36 |
NG_008975.1:g.21675G= , LRG_435:g.21675G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000432444.2:c.*1052G= | ENSP00000395617.1:n.*1052G= | |
ENST00000306077.5:c.1022G= MANE Select | ENSP00000303992.5:p.Arg341= | |
ENST00000306077.4:c.1022G= | ENSP00000303992.4:p.Arg341= | |
ENST00000601399.3:n.327+2317G= | ||
ENST00000608606.1:c.236+2317G= | ||
NM_024334.2:c.1022G= , LRG_435t1:c.1022G= | NP_077310.1:p.Arg341= | |
XM_011534109.1:c.917G= | XP_011532411.1:p.Arg306= | |
XM_017007176.2:c.917G= | XP_016862665.1:p.Arg306= | |
NM_024334.3:c.1022G= MANE Select | NP_077310.1:p.Arg341= |