HGVS | Genome Assembly |
---|---|
NC_000011.10:g.71454579A>G , CM000673.2:g.71454579A>G | GRCh38 |
NC_000011.9:g.71165625A>G , CM000673.1:g.71165625A>G | GRCh37 |
NC_000011.8:g.70843273A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000319023.7:c.86-531A>G MANE Select | ENSP00000326424.2:n.86-531A>G | |
ENST00000319023.6:c.86-531A>G | ENSP00000326424.2:n.86-531A>G | |
ENST00000524949.5:n.152-531A>G | ||
ENST00000525245.1:n.27-531A>G | ||
ENST00000527538.5:n.142-531A>G | ||
ENST00000528509.5:c.86-531A>G | ENSP00000433472.1:n.86-531A>G | |
ENST00000529120.5:c.86-531A>G | ENSP00000437220.1:n.86-531A>G | |
ENST00000533612.1:n.174-531A>G | ||
ENST00000533769.5:n.152-531A>G | ||
ENST00000534634.5:n.274-531A>G | ||
NM_018161.4:c.86-531A>G | NP_060631.2:n.86-531A>G | |
NM_018161.5:c.86-531A>G MANE Select | NP_060631.2:n.86-531A>G |