Canonical Allele Identifier:
CA1649498151
Gene:
Linked Data
dbSNP Id:
rs1772156166
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.98014560C>A , CM000668.2:g.98014560C>A | GRCh38 |
| NC_000006.11:g.98462436C>A , CM000668.1:g.98462436C>A | GRCh37 |
| NC_000006.10:g.98569157C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_245563.2:n.371+45094C>A | ||
| XR_942809.1:n.371+45094C>A |