HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52651993_52651995dup , CM000674.2:g.52651993_52651995dup | GRCh38 |
NC_000012.11:g.53045777_53045779dup , CM000674.1:g.53045777_53045779dup | GRCh37 |
NC_000012.10:g.51332044_51332046dup | NCBI36 |
NG_008296.1:g.5183_5185dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000309680.4:c.150_152dup MANE Select | ENSP00000310861.3:p.Gly51_Gly52insGly | |
ENST00000309680.3:c.150_152dup | ENSP00000310861.3:p.Gly51_Gly52insGly | |
NM_000423.2:c.150_152dup | NP_000414.2:p.Gly51_Gly52insGly | |
NM_000423.3:c.150_152dup MANE Select | NP_000414.2:p.Gly51_Gly52insGly |