HGVS | Genome Assembly |
---|---|
NC_000002.12:g.85589135_85589150delinsATTTATTCAGGAACTG , CM000664.2:g.85589135_85589150delinsATTTATTCAGGAACTG | GRCh38 |
NC_000002.11:g.85816258_85816273delinsATTTATTCAGGAACTG , CM000664.1:g.85816258_85816273delinsATTTATTCAGGAACTG | GRCh37 |
NC_000002.10:g.85669769_85669784delinsATTTATTCAGGAACTG | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000306384.5:c.4-2590_4-2575delinsATTTATTCAGGAACTG MANE Select | ENSP00000305647.4:n.4-2590_4-2575delinsAT... | |
ENST00000306384.4:c.4-2590_4-2575delinsATTTATTCAGGAACTG | ENSP00000305647.4:n.4-2590_4-2575delinsAT... | |
NM_006634.2:c.4-2590_4-2575delinsATTTATTCAGGAACTG | NP_006625.1:n.4-2590_4-2575delinsATTTATTC... | |
NM_006634.3:c.4-2590_4-2575delinsATTTATTCAGGAACTG MANE Select | NP_006625.1:n.4-2590_4-2575delinsATTTATTC... |