Canonical Allele Identifier:
CA1439212754
Gene:
Linked Data
dbSNP Id:
rs34353384
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.12578133C>A , CM000666.2:g.12578133C>A | GRCh38 |
| NC_000004.11:g.12579757C>A , CM000666.1:g.12579757C>A | GRCh37 |
| NC_000004.10:g.12188855C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_925406.1:n.106+31209G>T | ||
| XR_001741374.1:n.254+44522G>T | ||
| XR_925406.3:n.140+31209G>T |