HGVS | Genome Assembly |
---|---|
NC_000023.11:g.153736058_153736059delinsTG , CM000685.2:g.153736058_153736059delinsTG | GRCh38 |
NC_000023.10:g.153001512_153001513delinsTG , CM000685.1:g.153001512_153001513delinsTG | GRCh37 |
NC_000023.9:g.152654706_152654707delinsTG | NCBI36 |
NG_009022.2:g.16191_16192delinsTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000218104.6:c.1082-54_1082-53delinsTG MANE Select | ENSP00000218104.3:n.1082-54_1082-53delinsTG | |
ENST00000218104.5:c.1082-54_1082-53delinsTG | ENSP00000218104.3:n.1082-54_1082-53delinsTG | |
ENST00000443684.2:n.85-54_85-53delinsTG | ||
NM_000033.3:c.1082-54_1082-53delinsTG | NP_000024.2:n.1082-54_1082-53delinsTG | |
XR_938507.1:n.1498-54_1498-53delinsTG | ||
XR_938507.2:n.1498-54_1498-53delinsTG | ||
NM_000033.4:c.1082-54_1082-53delinsTG MANE Select | NP_000024.2:n.1082-54_1082-53delinsTG |