HGVS | Genome Assembly |
---|---|
NC_000003.12:g.49125411A>C , CM000665.2:g.49125411A>C | GRCh38 |
NC_000003.11:g.49162844A>C , CM000665.1:g.49162844A>C | GRCh37 |
NC_000003.10:g.49137848A>C | NCBI36 |
NG_008094.1:g.12756T>G | |
NG_054716.1:g.528T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305544.9:c.2562T>G MANE Select | ENSP00000307156.4:p.Thr854= | |
ENST00000305544.8:c.2562T>G | ENSP00000307156.4:p.Thr854= | |
ENST00000418109.5:c.2562T>G | ENSP00000388325.1:p.Thr854= | |
ENST00000464891.5:n.311T>G | ||
ENST00000477701.1:n.435T>G | ||
ENST00000483057.1:n.162T>G | ||
ENST00000486298.5:n.426-242T>G | ||
NM_002292.3:c.2562T>G | NP_002283.3:p.Thr854= | |
XM_005265127.3:c.2562T>G | XP_005265184.1:p.Thr854= | |
XM_005265127.4:c.2562T>G | XP_005265184.1:p.Thr854= | |
NM_002292.4:c.2562T>G MANE Select | NP_002283.3:p.Thr854= |