Canonical Allele Identifier:
CA1948159583
Gene:
Linked Data
dbSNP Id:
rs1589883718
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2444516A>G , CM000673.2:g.2444516A>G | GRCh38 |
| NC_000011.9:g.2465746A>G , CM000673.1:g.2465746A>G | GRCh37 |
| NC_000011.8:g.2422322A>G | NCBI36 |
| NG_008935.1:g.4526A>G , LRG_287:g.4526A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930984.1:n.55T>C |