HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23396648_23396649delinsAC , CM000676.2:g.23396648_23396649delinsAC | GRCh38 |
NC_000014.8:g.23865857_23865858delinsAC , CM000676.1:g.23865857_23865858delinsAC | GRCh37 |
NC_000014.7:g.22935697_22935698delinsAC | NCBI36 |
NG_023444.1:g.16629_16630delinsGT , LRG_389:g.16629_16630delinsGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000405093.9:c.2292+45_2292+46delinsGT MANE Select | ENSP00000386041.3:n.2292+45_2292+46delinsGT | |
ENST00000356287.3:c.2292+45_2292+46delinsGT | ENSP00000348634.3:n.2292+45_2292+46delinsGT | |
ENST00000405093.7:c.2292+45_2292+46delinsGT | ENSP00000386041.3:n.2292+45_2292+46delinsGT | |
NM_002471.3:c.2292+45_2292+46delinsGT , LRG_389t1:c.2292+45_2292+46delinsGT | NP_002462.2:n.2292+45_2292+46delinsGT | |
NM_002471.4:c.2292+45_2292+46delinsGT MANE Select | NP_002462.2:n.2292+45_2292+46delinsGT |