HGVS | Genome Assembly |
---|---|
NC_000006.12:g.123218744_123218745insACTGATG , CM000668.2:g.123218744_123218745insACTGATG | GRCh38 |
NC_000006.11:g.123539889_123539890insACTGATG , CM000668.1:g.123539889_123539890insACTGATG | GRCh37 |
NC_000006.10:g.123581588_123581589insACTGATG | NCBI36 |
NG_030438.1:g.423349_423350insCATCAGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000334268.9:c.2051-5_2051-4insCATCAGT MANE Select | ENSP00000333984.5:n.2051-5_2051-4insCATCAGT | |
ENST00000334268.8:c.2051-5_2051-4insCATCAGT | ENSP00000333984.5:n.2051-5_2051-4insCATCAGT | |
NM_006073.3:c.2051-5_2051-4insCATCAGT | NP_006064.2:n.2051-5_2051-4insCATCAGT | |
XM_011535382.1:c.1970-5_1970-4insCATCAGT | XP_011533684.1:n.1970-5_1970-4insCATCAGT | |
NM_006073.4:c.2051-5_2051-4insCATCAGT MANE Select | NP_006064.2:n.2051-5_2051-4insCATCAGT |