HGVS | Genome Assembly |
---|---|
NC_000001.11:g.183243097A>G , CM000663.2:g.183243097A>G | GRCh38 |
NC_000001.10:g.183212232A>G , CM000663.1:g.183212232A>G | GRCh37 |
NC_000001.9:g.181478855A>G | NCBI36 |
NG_007079.2:g.61834A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264144.5:c.3329-50A>G MANE Select | ENSP00000264144.4:n.3329-50A>G | |
ENST00000264144.4:c.3329-50A>G | ENSP00000264144.4:n.3329-50A>G | |
NM_005562.2:c.3329-50A>G | NP_005553.2:n.3329-50A>G | |
NM_005562.3:c.3329-50A>G MANE Select | NP_005553.2:n.3329-50A>G |