HGVS | Genome Assembly |
---|---|
NC_000015.10:g.59419493A>G , CM000677.2:g.59419493A>G | GRCh38 |
NC_000015.9:g.59711692A>G , CM000677.1:g.59711692A>G | GRCh37 |
NC_000015.8:g.57498984A>G | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000558348.5:c.-78+17135A>G | ENSP00000453918.1:n.-78+17135A>G | |
ENST00000560394.5:c.-78+17135A>G | ENSP00000452962.1:n.-78+17135A>G | |
XM_006720399.1:c.-78+17135A>G | XP_006720462.1:n.-78+17135A>G | |
XM_011521248.1:c.-22+17135A>G | XP_011519550.1:n.-22+17135A>G | |
XM_011521248.2:c.-22+17135A>G | XP_011519550.1:n.-22+17135A>G |