HGVS | Genome Assembly |
---|---|
NC_000006.12:g.1612842T>G , CM000668.2:g.1612842T>G | GRCh38 |
NC_000006.11:g.1613077T>G , CM000668.1:g.1613077T>G | GRCh37 |
NC_000006.10:g.1558076T>G | NCBI36 |
NG_009368.1:g.7397T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000645831.2:c.*735T>G MANE Select | ENSP00000493906.1:n.*735T>G | |
ENST00000380874.3:c.*735T>G | ENSP00000370256.2:n.*735T>G | |
NM_001453.2:c.2397T>G | NP_001444.2:n.2397T>G | |
NM_001453.3:c.*735T>G MANE Select | NP_001444.2:n.*735T>G |