Canonical Allele Identifier:
CA1481405851
Gene:
Linked Data
dbSNP Id:
rs1738891158
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.102499919dup , CM000666.2:g.102499919dup | GRCh38 |
| NC_000004.11:g.103421076dup , CM000666.1:g.103421076dup | GRCh37 |
| NC_000004.10:g.103640108dup | NCBI36 |
| NG_050628.1:g.3591dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011532467.1:c.643+1332dup | XP_011530769.1:n.643+1332dup | |
| NR_136202.1:n.48+2522dup |