HGVS | Genome Assembly |
---|---|
NC_000023.11:g.29917372A>G , CM000685.2:g.29917372A>G | GRCh38 |
NC_000023.10:g.29935489A>G , CM000685.1:g.29935489A>G | GRCh37 |
NC_000023.9:g.29845410A>G | NCBI36 |
NG_008292.1:g.1334809A>G | |
NG_008292.2:g.1334809A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378993.6:c.779-92A>G MANE Select | ENSP00000368278.1:n.779-92A>G | |
ENST00000378993.5:c.779-92A>G | ENSP00000368278.1:n.779-92A>G | |
NM_014271.3:c.779-92A>G | NP_055086.1:n.779-92A>G | |
XM_005274441.1:c.779-92A>G | XP_005274498.1:n.779-92A>G | |
XM_011545445.1:c.779-92A>G | XP_011543747.1:n.779-92A>G | |
XM_017029240.1:c.779-92A>G | XP_016884729.1:n.779-92A>G | |
XM_017029241.1:c.401-92A>G | XP_016884730.1:n.401-92A>G | |
NM_014271.4:c.779-92A>G MANE Select | NP_055086.1:n.779-92A>G |