HGVS | Genome Assembly |
---|---|
NC_000021.9:g.43416507_43416512dup , CM000683.2:g.43416507_43416512dup | GRCh38 |
NG_052009.1:g.15627_15632dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270162.8:c.*236_*241dup MANE Select | ENSP00000270162.6:n.*236_*241dup | |
ENST00000270162.6:c.*236_*241dup | ENSP00000270162.6:n.*236_*241dup | |
NM_173354.3:c.*236_*241dup | NP_775490.2:n.*236_*241dup | |
XM_011529474.1:c.*236_*241dup | XP_011527776.1:n.*236_*241dup | |
NM_173354.4:c.*236_*241dup | NP_775490.2:n.*236_*241dup | |
XM_011529474.2:c.*236_*241dup | XP_011527776.1:n.*236_*241dup | |
NM_173354.5:c.*236_*241dup MANE Select | NP_775490.2:n.*236_*241dup |