Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171652680_171652681insA , CM000663.2:g.171652680_171652681insA | GRCh38 |
| NC_000001.10:g.171621820_171621821insA , CM000663.1:g.171621820_171621821insA | GRCh37 |
| NC_000001.9:g.169888443_169888444insA | NCBI36 |
| NG_008859.1:g.4953_4954insT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.-70_-69insT MANE Select | ENSP00000037502.5:n.-70_-69insT | |
| ENST00000037502.10:c.-70_-69insT | ENSP00000037502.5:n.-70_-69insT | |
| NM_000261.2:c.-70_-69insT MANE Select | NP_000252.1:n.-70_-69insT |