HGVS | Genome Assembly |
---|---|
NC_000008.11:g.38148433dup , CM000670.2:g.38148433dup | GRCh38 |
NC_000008.10:g.38005951dup , CM000670.1:g.38005951dup | GRCh37 |
NC_000008.9:g.38125108dup | NCBI36 |
NG_011827.1:g.7650dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000276449.9:c.179-106dup MANE Select | ENSP00000276449.3:n.179-106dup | |
ENST00000276449.8:c.179-106dup | ENSP00000276449.3:n.179-106dup | |
ENST00000520114.1:n.560dup | ||
ENST00000521236.1:c.-100-74dup | ENSP00000430030.1:n.-100-74dup | |
ENST00000522050.1:c.115-106dup | ||
NM_000349.2:c.179-106dup | NP_000340.2:n.179-106dup | |
XM_006716392.1:c.179-106dup | XP_006716455.1:n.179-106dup | |
NM_000349.3:c.179-106dup MANE Select | NP_000340.2:n.179-106dup |