Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171652678_171652679insAG , CM000663.2:g.171652678_171652679insAG | GRCh38 |
| NC_000001.10:g.171621818_171621819insAG , CM000663.1:g.171621818_171621819insAG | GRCh37 |
| NC_000001.9:g.169888441_169888442insAG | NCBI36 |
| NG_008859.1:g.4955_4956insCT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.-68_-67insCT MANE Select | ENSP00000037502.5:n.-68_-67insCT | |
| ENST00000037502.10:c.-68_-67insCT | ENSP00000037502.5:n.-68_-67insCT | |
| NM_000261.2:c.-68_-67insCT MANE Select | NP_000252.1:n.-68_-67insCT |