Canonical Allele Identifier:
CA1481405842
Gene:
Linked Data
dbSNP Id:
rs1738890466
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.102499903G>A , CM000666.2:g.102499903G>A | GRCh38 |
| NC_000004.11:g.103421060G>A , CM000666.1:g.103421060G>A | GRCh37 |
| NC_000004.10:g.103640092G>A | NCBI36 |
| NG_050628.1:g.3575G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011532467.1:c.643+1346C>T | XP_011530769.1:n.643+1346C>T | |
| NR_136202.1:n.48+2536C>T |