HGVS | Genome Assembly |
---|---|
NC_000012.12:g.71983554_71983557delinsTCTC , CM000674.2:g.71983554_71983557delinsTCTC | GRCh38 |
NC_000012.11:g.72377334_72377337delinsTCTC , CM000674.1:g.72377334_72377337delinsTCTC | GRCh37 |
NC_000012.10:g.70663601_70663604delinsTCTC | NCBI36 |
NG_008279.1:g.49709_49712delinsTCTC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000333850.4:c.941+4467_941+4470delinsTCTC MANE Select | ENSP00000329093.3:n.941+4467_941+4470deli... | |
ENST00000333850.3:c.941+4467_941+4470delinsTCTC | ENSP00000329093.3:n.941+4467_941+4470deli... | |
NM_173353.3:c.941+4467_941+4470delinsTCTC | NP_775489.2:n.941+4467_941+4470delinsTCTC... | |
XM_011537899.1:c.347+4467_347+4470delinsTCTC | XP_011536201.1:n.347+4467_347+4470delinsT... | |
NM_173353.4:c.941+4467_941+4470delinsTCTC MANE Select | NP_775489.2:n.941+4467_941+4470delinsTCTC... |