HGVS | Genome Assembly |
---|---|
NC_000003.12:g.129529206_129529207insACT , CM000665.2:g.129529206_129529207insACT | GRCh38 |
NC_000003.11:g.129248049_129248050insACT , CM000665.1:g.129248049_129248050insACT | GRCh37 |
NC_000003.10:g.130730739_130730740insACT | NCBI36 |
NG_009115.1:g.5568_5569insACT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296271.4:c.361+112_361+113insACT MANE Select | ENSP00000296271.3:n.361+112_361+113insACT | |
ENST00000296271.3:c.361+112_361+113insACT | ENSP00000296271.3:n.361+112_361+113insACT | |
NM_000539.3:c.361+112_361+113insACT MANE Select | NP_000530.1:n.361+112_361+113insACT |