HGVS | Genome Assembly |
---|---|
NC_000001.11:g.97549561_97549562insACT , CM000663.2:g.97549561_97549562insACT | GRCh38 |
NC_000001.10:g.98015117_98015118insACT , CM000663.1:g.98015117_98015118insACT | GRCh37 |
NC_000001.9:g.97787705_97787706insACT | NCBI36 |
NG_008807.2:g.376500_376501insTAG , LRG_722:g.376500_376501insTAG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370192.8:c.1524_1524+1insTAG | ||
ENST00000370192.7:c.1524_1524+1insTAG | ||
NM_000110.3:c.1524_1524+1insTAG , LRG_722t1:c.1524_1524+1insTAG | ||
XM_005270562.3:c.1524_1524+1insTAG | ||
XM_006710397.2:c.1524_1524+1insTAG | ||
XM_006710397.3:c.1524_1524+1insTAG | ||
XM_017000507.1:c.1413_1413+1insTAG | ||
XM_017000508.2:c.1029_1029+1insTAG | ||
XM_017000509.2:c.1029_1029+1insTAG | ||
XM_017000510.1:c.1029_1029+1insTAG | ||
NM_000110.4:c.1524_1524+1insTAG |