HGVS | Genome Assembly |
---|---|
NC_000006.12:g.29945987_29945988insCTGT , CM000668.2:g.29945987_29945988insCTGT | GRCh38 |
NC_000006.11:g.29913764_29913765insCTGT , CM000668.1:g.29913764_29913765insCTGT | GRCh37 |
NC_000006.10:g.30021743_30021744insCTGT | NCBI36 |
NG_029217.2:g.8523_8524insCTGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706901.1:c.*532_*533insCTGT | ENSP00000516612.1:n.*532_*533insCTGT | |
ENST00000706902.1:c.1093+706_1093+707insCTGT | ENSP00000516613.1:n.1093+706_1093+707insCTGT | |
ENST00000706903.1:c.*124+408_*124+409insCTGT | ENSP00000516614.1:n.*124+408_*124+409insCTGT | |
ENST00000706904.1:c.1093+706_1093+707insCTGT | ENSP00000516615.1:n.1093+706_1093+707insCTGT | |
ENST00000706905.1:c.*532_*533insCTGT | ENSP00000516616.1:n.*532_*533insCTGT |