HGVS | Genome Assembly |
---|---|
NC_000023.11:g.78118204_78118205insG , CM000685.2:g.78118204_78118205insG | GRCh38 |
NC_000023.10:g.77373701_77373702insG , CM000685.1:g.77373701_77373702insG | GRCh37 |
NC_000023.9:g.77260357_77260358insG | NCBI36 |
NG_008862.1:g.19036_19037insG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373316.5:c.641+34_641+35insG MANE Select | ENSP00000362413.4:n.641+34_641+35insG | |
ENST00000644362.1:c.557+34_557+35insG | ENSP00000496140.1:n.557+34_557+35insG | |
ENST00000373316.4:c.641+34_641+35insG | ENSP00000362413.4:n.641+34_641+35insG | |
ENST00000491291.1:n.633+34_633+35insG | ||
NM_000291.3:c.641+34_641+35insG | NP_000282.1:n.641+34_641+35insG | |
NM_000291.4:c.641+34_641+35insG MANE Select | NP_000282.1:n.641+34_641+35insG |