HGVS | Genome Assembly |
---|---|
NC_000012.12:g.63146853_63146854dup , CM000674.2:g.63146853_63146854dup | GRCh38 |
NC_000012.11:g.63540633_63540634dup , CM000674.1:g.63540633_63540634dup | GRCh37 |
NC_000012.10:g.61826900_61826901dup | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299178.4:c.*505_*506dup MANE Select | ENSP00000299178.3:n.*505_*506dup | |
ENST00000299178.3:c.*505_*506dup | ENSP00000299178.2:n.*505_*506dup | |
ENST00000550940.1:c.538+567_538+568dup | ENSP00000449822.1:n.538+567_538+568dup | |
NM_000706.4:c.*505_*506dup | NP_000697.1:n.*505_*506dup | |
XM_005269002.3:c.*505_*506dup | XP_005269059.1:n.*505_*506dup | |
NM_000706.5:c.*505_*506dup MANE Select | NP_000697.1:n.*505_*506dup |