HGVS | Genome Assembly |
---|---|
NC_000022.11:g.32104847A>T , CM000684.2:g.32104847A>T | GRCh38 |
NC_000022.10:g.32500834A>T , CM000684.1:g.32500834A>T | GRCh37 |
NC_000022.9:g.30830834A>T | NCBI36 |
NG_017045.1:g.66816A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266088.9:c.1727A>T MANE Select | ENSP00000266088.4:p.Glu576Val | |
ENST00000266088.8:c.1727A>T | ENSP00000266088.4:p.Glu576Val | |
ENST00000543737.2:c.1346A>T | ENSP00000444898.1:p.Glu449Val | |
NM_000343.3:c.1727A>T | NP_000334.1:p.Glu576Val | |
NM_001256314.1:c.1346A>T | NP_001243243.1:p.Glu449Val | |
XR_938173.1:n.591+1991T>A | ||
XR_938174.1:n.486+15008T>A | ||
NM_000343.4:c.1727A>T MANE Select | NP_000334.1:p.Glu576Val | |
NM_001256314.2:c.1346A>T | NP_001243243.1:p.Glu449Val |