Canonical Allele Identifier:
CA1649498097
Gene:
Linked Data
dbSNP Id:
rs1772155757
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.98014483C>G , CM000668.2:g.98014483C>G | GRCh38 |
| NC_000006.11:g.98462359C>G , CM000668.1:g.98462359C>G | GRCh37 |
| NC_000006.10:g.98569080C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_245563.2:n.371+45017C>G | ||
| XR_942809.1:n.371+45017C>G |