HGVS | Genome Assembly |
---|---|
NC_000023.11:g.68829765_68829766delinsGC , CM000685.2:g.68829765_68829766delinsGC | GRCh38 |
NC_000023.10:g.68049608_68049609delinsGC , CM000685.1:g.68049608_68049609delinsGC | GRCh37 |
NC_000023.9:g.67966333_67966334delinsGC | NCBI36 |
NG_008887.1:g.5769_5770delinsGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000204961.5:c.-12_-11delinsGC MANE Select | ENSP00000204961.4:n.-12_-11delinsGC | |
ENST00000204961.4:c.-12_-11delinsGC | ENSP00000204961.4:n.-12_-11delinsGC | |
NM_004429.4:c.-12_-11delinsGC | NP_004420.1:n.-12_-11delinsGC | |
NM_004429.5:c.-12_-11delinsGC MANE Select | NP_004420.1:n.-12_-11delinsGC |