Linked Data
gnomAD v2:
12-111155080-T-TA
MyVariant Identifiers:
chr12:g.111155080_111155081insA (hg19)
chr12:g.110717275_110717276insA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.110717275_110717276insA , CM000674.2:g.110717275_110717276insA | GRCh38 |
| NC_000012.11:g.111155080_111155081insA , CM000674.1:g.111155080_111155081insA | GRCh37 |
| NC_000012.10:g.109639463_109639464insA | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011538504.1:c.944-2129_944-2128insT | XP_011536806.1:n.944-2129_944-2128insT | |
| XM_011538505.1:c.943+3829_943+3830insT | XP_011536807.1:n.943+3829_943+3830insT | |
| XM_011538504.3:c.944-2129_944-2128insT | XP_011536806.1:n.944-2129_944-2128insT | |
| XM_011538505.3:c.943+3829_943+3830insT | XP_011536807.1:n.943+3829_943+3830insT |