HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23431583_23431584delinsAC , CM000676.2:g.23431583_23431584delinsAC | GRCh38 |
NC_000014.8:g.23900792_23900793delinsAC , CM000676.1:g.23900792_23900793delinsAC | GRCh37 |
NC_000014.7:g.22970632_22970633delinsAC | NCBI36 |
NG_007884.1:g.9078_9079delinsGT , LRG_384:g.9078_9079delinsGT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000355349.4:c.732+1_732+2delinsGT MANE Select | ENSP00000347507.3:n.732+1_732+2delinsGT | |
ENST00000355349.3:c.732+1_732+2delinsGT | ENSP00000347507.3:n.732+1_732+2delinsGT | |
NM_000257.3:c.732+1_732+2delinsGT | NP_000248.2:n.732+1_732+2delinsGT | |
XR_245686.3:n.838+1_838+2delinsGT | ||
XM_017021340.1:c.732+1_732+2delinsGT | XP_016876829.1:n.732+1_732+2delinsGT | |
NM_000257.4:c.732+1_732+2delinsGT MANE Select | NP_000248.2:n.732+1_732+2delinsGT |