Canonical Allele Identifier:
CA1481405789
Gene:
Linked Data
dbSNP Id:
rs1738886466
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.102499860_102499861insG , CM000666.2:g.102499860_102499861insG | GRCh38 |
| NC_000004.11:g.103421017_103421018insG , CM000666.1:g.103421017_103421018insG | GRCh37 |
| NC_000004.10:g.103640049_103640050insG | NCBI36 |
| NG_050628.1:g.3532_3533insG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011532467.1:c.643+1388_643+1389insC | XP_011530769.1:n.643+1388_643+1389insC | |
| NR_136202.1:n.48+2578_48+2579insC |