Canonical Allele Identifier:
CA1649498098
Gene:
Linked Data
dbSNP Id:
rs1772155797
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.98014491T>C , CM000668.2:g.98014491T>C | GRCh38 |
| NC_000006.11:g.98462367T>C , CM000668.1:g.98462367T>C | GRCh37 |
| NC_000006.10:g.98569088T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_245563.2:n.371+45025T>C | ||
| XR_942809.1:n.371+45025T>C |