HGVS | Genome Assembly |
---|---|
NC_000003.12:g.129529238_129529239insA , CM000665.2:g.129529238_129529239insA | GRCh38 |
NC_000003.11:g.129248081_129248082insA , CM000665.1:g.129248081_129248082insA | GRCh37 |
NC_000003.10:g.130730771_130730772insA | NCBI36 |
NG_009115.1:g.5600_5601insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296271.4:c.361+144_361+145insA MANE Select | ENSP00000296271.3:n.361+144_361+145insA | |
ENST00000296271.3:c.361+144_361+145insA | ENSP00000296271.3:n.361+144_361+145insA | |
NM_000539.3:c.361+144_361+145insA MANE Select | NP_000530.1:n.361+144_361+145insA |