HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189007420dup , CM000664.2:g.189007420dup | GRCh38 |
NC_000002.11:g.189872146dup , CM000664.1:g.189872146dup | GRCh37 |
NC_000002.10:g.189580391dup | NCBI36 |
NG_007404.1:g.38048dup , LRG_3:g.38048dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000450867.2:c.3157-80dup | ENSP00000415346.2:n.3157-80dup | |
ENST00000304636.9:c.3256-80dup MANE Select | ENSP00000304408.4:n.3256-80dup | |
ENST00000304636.7:c.3256-80dup | ENSP00000304408.3:n.3256-80dup | |
ENST00000317840.9:c.2528-634dup | ENSP00000315243.6:n.2528-634dup | |
NM_000090.3:c.3256-80dup , LRG_3t1:c.3256-80dup | NP_000081.1:n.3256-80dup | |
NM_000090.4:c.3256-80dup MANE Select | NP_000081.2:n.3256-80dup |