HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23424489_23424490delinsAG , CM000676.2:g.23424489_23424490delinsAG | GRCh38 |
NC_000014.8:g.23893698_23893699delinsAG , CM000676.1:g.23893698_23893699delinsAG | GRCh37 |
NC_000014.7:g.22963538_22963539delinsAG | NCBI36 |
NG_007884.1:g.16172_16173delinsCT , LRG_384:g.16172_16173delinsCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.2679+279_2679+280delinsCT MANE Select | ENSP00000347507.3:n.2679+279_2679+280delinsCT | |
ENST00000355349.3:c.2679+279_2679+280delinsCT | ENSP00000347507.3:n.2679+279_2679+280delinsCT | |
NM_000257.3:c.2679+279_2679+280delinsCT | NP_000248.2:n.2679+279_2679+280delinsCT | |
XR_245686.3:n.2785+279_2785+280delinsCT | ||
XM_017021340.1:c.2679+279_2679+280delinsCT | XP_016876829.1:n.2679+279_2679+280delinsCT | |
NM_000257.4:c.2679+279_2679+280delinsCT MANE Select | NP_000248.2:n.2679+279_2679+280delinsCT |