Canonical Allele Identifier:
CA1833676291
Gene:
Linked Data
dbSNP Id:
rs1213129874
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.12108925C>A , CM000671.2:g.12108925C>A | GRCh38 |
| NC_000009.11:g.12108925C>A , CM000671.1:g.12108925C>A | GRCh37 |
| NC_000009.10:g.12098925C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_929481.1:n.166+7896G>T | ||
| XR_929482.1:n.260+7896G>T | ||
| XR_929481.2:n.166+7896G>T | ||
| XR_929482.2:n.260+7896G>T |