HGVS | Genome Assembly |
---|---|
NC_000012.12:g.69353295dup , CM000674.2:g.69353295dup | GRCh38 |
NC_000012.11:g.69747075dup , CM000674.1:g.69747075dup | GRCh37 |
NC_000012.10:g.68033342dup | NCBI36 |
NG_008195.1:g.9942dup , LRG_768:g.9942dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261267.7:c.*76dup MANE Select | ENSP00000261267.2:n.*76dup | |
ENST00000261267.6:c.*76dup | ENSP00000261267.2:n.*76dup | |
ENST00000549690.1:c.*30dup | ENSP00000449898.1:n.*30dup | |
NM_000239.2:c.*76dup , LRG_768t1:c.*76dup | NP_000230.1:n.*76dup | |
NM_000239.3:c.*76dup MANE Select | NP_000230.1:n.*76dup |