Canonical Allele Identifier:
CA1948159655
Gene:
Linked Data
dbSNP Id:
rs1845998461
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2444567G>C , CM000673.2:g.2444567G>C | GRCh38 |
| NC_000011.9:g.2465797G>C , CM000673.1:g.2465797G>C | GRCh37 |
| NC_000011.8:g.2422373G>C | NCBI36 |
| NG_008935.1:g.4577G>C , LRG_287:g.4577G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930984.1:n.4C>G |