HGVS | Genome Assembly |
---|---|
NC_000006.12:g.1612868G>T , CM000668.2:g.1612868G>T | GRCh38 |
NC_000006.11:g.1613103G>T , CM000668.1:g.1613103G>T | GRCh37 |
NC_000006.10:g.1558102G>T | NCBI36 |
NG_009368.1:g.7423G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000645831.2:c.*761G>T MANE Select | ENSP00000493906.1:n.*761G>T | |
ENST00000380874.3:c.*761G>T | ENSP00000370256.2:n.*761G>T | |
NM_001453.2:c.2423G>T | NP_001444.2:n.2423G>T | |
NM_001453.3:c.*761G>T MANE Select | NP_001444.2:n.*761G>T |