Canonical Allele Identifier:
CA1963413318
Gene:
Linked Data
dbSNP Id:
rs1851775129
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.34812513G>C , CM000673.2:g.34812513G>C | GRCh38 |
| NC_000011.9:g.34834060G>C , CM000673.1:g.34834060G>C | GRCh37 |
| NC_000011.8:g.34790636G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_428897.2:n.579+57906G>C | ||
| XR_931188.1:n.693+57906G>C | ||
| XR_931189.1:n.854+57906G>C | ||
| XR_931190.1:n.639+57906G>C | ||
| XR_931191.1:n.689+57906G>C | ||
| XR_001748174.1:n.855+57906G>C | ||
| XR_001748176.1:n.1016+57906G>C | ||
| XR_002957246.1:n.639+57906G>C |