Canonical Allele Identifier:
CA1481405822
Gene:
Linked Data
dbSNP Id:
rs1738888714
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.102499883G>C , CM000666.2:g.102499883G>C | GRCh38 |
| NC_000004.11:g.103421040G>C , CM000666.1:g.103421040G>C | GRCh37 |
| NC_000004.10:g.103640072G>C | NCBI36 |
| NG_050628.1:g.3555G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011532467.1:c.643+1366C>G | XP_011530769.1:n.643+1366C>G | |
| NR_136202.1:n.48+2556C>G |