HGVS | Genome Assembly |
---|---|
NC_000023.11:g.139562122C>A , CM000685.2:g.139562122C>A | GRCh38 |
NC_000023.10:g.138644281C>A , CM000685.1:g.138644281C>A | GRCh37 |
NC_000023.9:g.138471947C>A | NCBI36 |
NG_007994.1:g.36387C>A , LRG_556:g.36387C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000218099.7:c.*51C>A MANE Select | ENSP00000218099.2:n.*51C>A | |
ENST00000643157.1:n.1723+381C>A | ||
ENST00000218099.6:c.*51C>A | ENSP00000218099.2:n.*51C>A | |
NM_000133.3:c.*51C>A , LRG_556t1:c.*51C>A | NP_000124.1:n.*51C>A | |
NM_001313913.1:c.*51C>A | NP_001300842.1:n.*51C>A | |
XM_005262397.3:c.*51C>A | XP_005262454.1:n.*51C>A | |
XM_005262397.4:c.*51C>A | XP_005262454.1:n.*51C>A | |
NM_000133.4:c.*51C>A MANE Select | NP_000124.1:n.*51C>A | |
NM_001313913.2:c.*51C>A | NP_001300842.1:n.*51C>A |