Canonical Allele Identifier:
CA1284674030
Gene:
Linked Data
dbSNP Id:
rs1573478963
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.122883843G>C , CM000664.2:g.122883843G>C | GRCh38 |
| NC_000002.11:g.123641419G>C , CM000664.1:g.123641419G>C | GRCh37 |
| NC_000002.10:g.123357889G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923292.1:n.1125-1099G>C | ||
| XR_001739692.1:n.1451-1099G>C | ||
| XR_923292.2:n.1358-1099G>C |