HGVS | Genome Assembly |
---|---|
NC_000005.10:g.173232610T>A , CM000667.2:g.173232610T>A | GRCh38 |
NC_000005.9:g.172659613T>A , CM000667.1:g.172659613T>A | GRCh37 |
NC_000005.8:g.172592219T>A | NCBI36 |
NG_013340.1:g.7703A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000329198.5:c.934A>T MANE Select | ENSP00000327758.4:p.Asn312Tyr | |
ENST00000329198.4:c.934A>T | ENSP00000327758.4:p.Asn312Tyr | |
NM_001166175.1:c.*887A>T | NP_001159647.1:n.*887A>T | |
NM_001166176.1:c.*733A>T | NP_001159648.1:n.*733A>T | |
NM_004387.3:c.934A>T | NP_004378.1:p.Asn312Tyr | |
NM_004387.4:c.934A>T MANE Select | NP_004378.1:p.Asn312Tyr | |
NM_001166175.2:c.*887A>T | NP_001159647.1:n.*887A>T | |
NM_001166176.2:c.*733A>T | NP_001159648.1:n.*733A>T |