HGVS | Genome Assembly |
---|---|
NC_000002.12:g.188988054dup , CM000664.2:g.188988054dup | GRCh38 |
NC_000002.11:g.189852780dup , CM000664.1:g.189852780dup | GRCh37 |
NC_000002.10:g.189561025dup | NCBI36 |
NG_007404.1:g.18682dup , LRG_3:g.18682dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000450867.2:c.529-27dup | ENSP00000415346.2:n.529-27dup | |
ENST00000304636.9:c.529-27dup MANE Select | ENSP00000304408.4:n.529-27dup | |
ENST00000304636.7:c.529-27dup | ENSP00000304408.3:n.529-27dup | |
ENST00000317840.9:c.529-27dup | ENSP00000315243.6:n.529-27dup | |
NM_000090.3:c.529-27dup , LRG_3t1:c.529-27dup | NP_000081.1:n.529-27dup | |
NM_000090.4:c.529-27dup MANE Select | NP_000081.2:n.529-27dup |