HGVS | Genome Assembly |
---|---|
NC_000011.10:g.8089928G>A , CM000673.2:g.8089928G>A | GRCh38 |
NC_000011.9:g.8111475G>A , CM000673.1:g.8111475G>A | GRCh37 |
NC_000011.8:g.8068051G>A | NCBI36 |
NG_029912.1:g.56296G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299506.3:c.91-141G>A MANE Select | ENSP00000299506.3:n.91-141G>A | |
ENST00000299506.2:c.91-141G>A | ENSP00000299506.2:n.91-141G>A | |
ENST00000305253.8:c.256-141G>A | ENSP00000305426.4:n.256-141G>A | |
ENST00000534099.5:c.109-141G>A | ENSP00000434400.1:n.109-141G>A | |
NM_003320.4:c.256-141G>A | NP_003311.2:n.256-141G>A | |
NM_177972.2:c.91-141G>A | NP_813977.1:n.91-141G>A | |
XM_005253109.2:c.217-141G>A | XP_005253166.1:n.217-141G>A | |
XM_011520344.1:c.127-141G>A | XP_011518646.1:n.127-141G>A | |
XM_005253109.3:c.217-141G>A | XP_005253166.1:n.217-141G>A | |
XM_011520344.2:c.127-141G>A | XP_011518646.1:n.127-141G>A | |
NM_177972.3:c.91-141G>A MANE Select | NP_813977.1:n.91-141G>A | |
NM_003320.5:c.256-141G>A | NP_003311.2:n.256-141G>A |