HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1411875_1411904dup , CM000667.2:g.1411875_1411904dup | GRCh38 |
NC_000005.9:g.1411990_1412019dup , CM000667.1:g.1411990_1412019dup | GRCh37 |
NC_000005.8:g.1464990_1465019dup | NCBI36 |
NG_015885.1:g.38659_38688dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000270349.12:c.1157-415_1157-386dup MANE Select | ENSP00000270349.9:n.1157-415_1157-386dup | |
ENST00000270349.11:c.1157-415_1157-386dup | ENSP00000270349.9:n.1157-415_1157-386dup | |
NM_001044.4:c.1157-415_1157-386dup | NP_001035.1:n.1157-415_1157-386dup | |
NM_001044.5:c.1157-415_1157-386dup MANE Select | NP_001035.1:n.1157-415_1157-386dup |