HGVS | Genome Assembly |
---|---|
NC_000017.11:g.63606301T>G , CM000679.2:g.63606301T>G | GRCh38 |
NC_000017.10:g.61683661T>G , CM000679.1:g.61683661T>G | GRCh37 |
NC_000017.9:g.59037393T>G | NCBI36 |
NG_016979.1:g.10431T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000682060.1:n.150-12T>G | ||
ENST00000684587.1:c.385-12T>G | ENSP00000507435.1:n.385-12T>G | |
ENST00000690765.1:c.*214-12T>G | ENSP00000510085.1:n.*214-12T>G | |
ENST00000258975.7:c.388-12T>G MANE Select | ENSP00000258975.6:n.388-12T>G | |
ENST00000258975.6:c.388-12T>G | ENSP00000258975.6:n.388-12T>G | |
ENST00000581120.1:n.590-12T>G | ||
NM_016360.3:c.388-12T>G | NP_057444.2:n.388-12T>G | |
NM_016360.4:c.388-12T>G MANE Select | NP_057444.2:n.388-12T>G |