HGVS | Genome Assembly |
---|---|
NC_000002.12:g.44942123dup , CM000664.2:g.44942123dup | GRCh38 |
NC_000002.11:g.45169262dup , CM000664.1:g.45169262dup | GRCh37 |
NC_000002.10:g.45022766dup | NCBI36 |
NG_016222.1:g.5226dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260653.5:c.19dup MANE Select | ENSP00000260653.3:p.Leu7ProfsTer26 | |
ENST00000260653.4:c.19dup | ENSP00000260653.3:p.Leu7ProfsTer26 | |
NM_005413.3:c.19dup | NP_005404.1:p.Leu7ProfsTer26 | |
XM_011533042.1:c.19dup | XP_011531344.1:p.Leu7ProfsTer26 | |
NM_005413.4:c.19dup MANE Select | NP_005404.1:p.Leu7ProfsTer26 |