HGVS | Genome Assembly |
---|---|
NC_000001.11:g.193251435G= , CM000663.2:g.193251435G= | GRCh38 |
NC_000001.10:g.193220565G= , CM000663.1:g.193220565G= | GRCh37 |
NC_000001.9:g.191487188G= | NCBI36 |
NG_012691.1:g.134478G= , LRG_507:g.134478G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367435.5:c.*723G= MANE Select | ENSP00000356405.4:n.*723G= | |
ENST00000635846.1:c.*723G= | ENSP00000490035.1:n.*723G= | |
ENST00000643006.1:c.*1229G= | ENSP00000496633.1:n.*1229G= | |
ENST00000367435.3:c.*723G= | ENSP00000356405.3:n.*723G= | |
NM_024529.4:c.*723G= , LRG_507t1:c.*723G= | NP_078805.3:n.*723G= | |
NM_024529.5:c.*723G= MANE Select | NP_078805.3:n.*723G= |