HGVS | Genome Assembly |
---|---|
NC_000004.12:g.46993540_46993555dup , CM000666.2:g.46993540_46993555dup | GRCh38 |
NC_000004.11:g.46995557_46995572dup , CM000666.1:g.46995557_46995572dup | GRCh37 |
NC_000004.10:g.46690314_46690329dup | NCBI36 |
NG_011809.1:g.5017_5032dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264318.4:c.-123_-108dup MANE Select | ENSP00000264318.3:n.-123_-108dup | |
ENST00000264318.3:c.-123_-108dup | ENSP00000264318.3:n.-123_-108dup | |
NM_000809.3:c.-123_-108dup | NP_000800.2:n.-123_-108dup | |
XM_011513677.1:c.-123_-108dup | XP_011511979.1:n.-123_-108dup | |
NM_000809.4:c.-123_-108dup MANE Select | NP_000800.2:n.-123_-108dup | |
NM_001204266.2:c.-112_-97dup | NP_001191195.1:n.-112_-97dup | |
NM_001204267.2:c.-112_-97dup | NP_001191196.1:n.-112_-97dup |