HGVS | Genome Assembly |
---|---|
NC_000004.12:g.67740084_67740087dup , CM000666.2:g.67740084_67740087dup | GRCh38 |
NC_000004.11:g.68605802_68605805dup , CM000666.1:g.68605802_68605805dup | GRCh37 |
NC_000004.10:g.68288397_68288400dup | NCBI36 |
NG_009293.1:g.21002_21005dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000226413.5:c.*395_*398dup MANE Select | ENSP00000226413.5:n.*395_*398dup | |
ENST00000226413.4:c.*395_*398dup | ENSP00000226413.4:n.*395_*398dup | |
NM_000406.2:c.*395_*398dup | NP_000397.1:n.*395_*398dup | |
NM_001012763.1:c.*504_*507dup | NP_001012781.1:n.*504_*507dup | |
NM_000406.3:c.*395_*398dup MANE Select | NP_000397.1:n.*395_*398dup | |
NM_001012763.2:c.*504_*507dup | NP_001012781.1:n.*504_*507dup |