HGVS | Genome Assembly |
---|---|
NC_000001.11:g.193251484G>T , CM000663.2:g.193251484G>T | GRCh38 |
NC_000001.10:g.193220614G>T , CM000663.1:g.193220614G>T | GRCh37 |
NC_000001.9:g.191487237G>T | NCBI36 |
NG_012691.1:g.134527G>T , LRG_507:g.134527G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367435.5:c.*772G>T MANE Select | ENSP00000356405.4:n.*772G>T | |
ENST00000635846.1:c.*772G>T | ENSP00000490035.1:n.*772G>T | |
ENST00000643006.1:c.*1278G>T | ENSP00000496633.1:n.*1278G>T | |
ENST00000367435.3:c.*772G>T | ENSP00000356405.3:n.*772G>T | |
NM_024529.4:c.*772G>T , LRG_507t1:c.*772G>T | NP_078805.3:n.*772G>T | |
NM_024529.5:c.*772G>T MANE Select | NP_078805.3:n.*772G>T |