Canonical Allele Identifier:
CA1439212900
Gene:
Linked Data
dbSNP Id:
rs115411483
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.12578262A>G , CM000666.2:g.12578262A>G | GRCh38 |
| NC_000004.11:g.12579886A>G , CM000666.1:g.12579886A>G | GRCh37 |
| NC_000004.10:g.12188984A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_925406.1:n.106+31080T>C | ||
| XR_001741374.1:n.254+44393T>C | ||
| XR_925406.3:n.140+31080T>C |