Canonical Allele Identifier:
CA1929213146
Gene:
Linked Data
dbSNP Id:
rs183776188
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94762334C>A , CM000672.2:g.94762334C>A | GRCh38 |
| NC_000010.10:g.96522091C>A , CM000672.1:g.96522091C>A | GRCh37 |
| NC_000010.9:g.96512081C>A | NCBI36 |
| NG_008384.2:g.4629C>A | |
| NG_008384.3:g.4654C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000464755.1:c.932-12724C>A | ENSP00000483243.1:n.932-12724C>A |