HGVS | Genome Assembly |
---|---|
NC_000012.12:g.69353329dup , CM000674.2:g.69353329dup | GRCh38 |
NC_000012.11:g.69747109dup , CM000674.1:g.69747109dup | GRCh37 |
NC_000012.10:g.68033376dup | NCBI36 |
NG_008195.1:g.9976dup , LRG_768:g.9976dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261267.7:c.*110dup MANE Select | ENSP00000261267.2:n.*110dup | |
ENST00000261267.6:c.*110dup | ENSP00000261267.2:n.*110dup | |
ENST00000549690.1:c.*64dup | ENSP00000449898.1:n.*64dup | |
NM_000239.2:c.*110dup , LRG_768t1:c.*110dup | NP_000230.1:n.*110dup | |
NM_000239.3:c.*110dup MANE Select | NP_000230.1:n.*110dup |