Canonical Allele Identifier:
CA1677169880
Gene:
Linked Data
dbSNP Id:
rs1582912285
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.160668467C>T , CM000668.2:g.160668467C>T | GRCh38 |
| NC_000006.11:g.161089499C>T , CM000668.1:g.161089499C>T | GRCh37 |
| NC_000006.10:g.161009489C>T | NCBI36 |
| NG_016147.1:g.2909G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452651.1:n.115-2094G>A |