HGVS | Genome Assembly |
---|---|
NC_000022.11:g.32104879A>T , CM000684.2:g.32104879A>T | GRCh38 |
NC_000022.10:g.32500866A>T , CM000684.1:g.32500866A>T | GRCh37 |
NC_000022.9:g.30830866A>T | NCBI36 |
NG_017045.1:g.66848A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266088.9:c.1759A>T MANE Select | ENSP00000266088.4:p.Thr587Ser | |
ENST00000266088.8:c.1759A>T | ENSP00000266088.4:p.Thr587Ser | |
ENST00000543737.2:c.1378A>T | ENSP00000444898.1:p.Thr460Ser | |
NM_000343.3:c.1759A>T | NP_000334.1:p.Thr587Ser | |
NM_001256314.1:c.1378A>T | NP_001243243.1:p.Thr460Ser | |
XR_938173.1:n.591+1959T>A | ||
XR_938174.1:n.486+14976T>A | ||
NM_000343.4:c.1759A>T MANE Select | NP_000334.1:p.Thr587Ser | |
NM_001256314.2:c.1378A>T | NP_001243243.1:p.Thr460Ser |