HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4631963T>C , CM000679.2:g.4631963T>C | GRCh38 |
NC_000017.10:g.4535258T>C , CM000679.1:g.4535258T>C | GRCh37 |
NC_000017.9:g.4482007T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293761.8:c.1735A>G MANE Select | ENSP00000293761.3:p.Thr579Ala | |
ENST00000570836.6:c.1735A>G | ENSP00000458832.1:p.Thr579Ala | |
ENST00000293761.7:c.1735A>G | ENSP00000293761.3:p.Thr579Ala | |
ENST00000570836.5:c.1735A>G | ENSP00000458832.1:p.Thr579Ala | |
ENST00000574640.1:c.1618A>G | ENSP00000460483.1:p.Thr540Ala | |
NM_001140.3:c.1735A>G | NP_001131.3:p.Thr579Ala | |
NM_001140.4:c.1735A>G | NP_001131.3:p.Thr579Ala | |
NM_001140.5:c.1735A>G MANE Select | NP_001131.3:p.Thr579Ala |