HGVS | Genome Assembly |
---|---|
NC_000018.10:g.905124A>G , CM000680.2:g.905124A>G | GRCh38 |
NC_000018.9:g.905125A>G , CM000680.1:g.905125A>G | GRCh37 |
NC_000018.8:g.895125A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000450565.8:c.-2+64A>G MANE Select | ENSP00000411658.3:n.-2+64A>G | |
ENST00000450565.7:c.-2+64A>G | ENSP00000411658.3:n.-2+64A>G | |
ENST00000579794.1:c.-263A>G | ENSP00000462647.1:n.-263A>G | |
NM_001099733.1:c.-2+64A>G | NP_001093203.1:n.-2+64A>G | |
XM_005258081.2:c.482+64A>G | XP_005258138.1:n.482+64A>G | |
XM_005258081.4:c.416+64A>G | XP_005258138.2:n.416+64A>G | |
NM_001099733.2:c.-2+64A>G MANE Select | NP_001093203.1:n.-2+64A>G |