HGVS | Genome Assembly |
---|---|
NC_000003.12:g.129528708_129528709insG , CM000665.2:g.129528708_129528709insG | GRCh38 |
NC_000003.11:g.129247551_129247552insG , CM000665.1:g.129247551_129247552insG | GRCh37 |
NC_000003.10:g.130730241_130730242insG | NCBI36 |
NG_009115.1:g.5070_5071insG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296271.4:c.-26_-25insG MANE Select | ENSP00000296271.3:n.-26_-25insG | |
ENST00000296271.3:c.-26_-25insG | ENSP00000296271.3:n.-26_-25insG | |
NM_000539.3:c.-26_-25insG MANE Select | NP_000530.1:n.-26_-25insG |