HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149927543dup , CM000663.2:g.149927543dup | GRCh38 |
NC_000001.10:g.149899435dup , CM000663.1:g.149899435dup | GRCh37 |
NC_000001.9:g.148166059dup | NCBI36 |
NG_032777.1:g.5711dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271628.9:c.34+184dup MANE Select | ENSP00000271628.8:n.34+184dup | |
ENST00000271628.8:c.34+184dup | ENSP00000271628.8:n.34+184dup | |
ENST00000457312.1:c.-206dup | ENSP00000391114.1:n.-206dup | |
NM_005850.4:c.34+184dup | NP_005841.1:n.34+184dup | |
NM_005850.5:c.34+184dup MANE Select | NP_005841.1:n.34+184dup |