Canonical Allele Identifier:
CA1595159115
Gene:
Linked Data
dbSNP Id:
rs10065906
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159580770C>G , CM000667.2:g.159580770C>G | GRCh38 |
| NC_000005.9:g.159007778C>G , CM000667.1:g.159007778C>G | GRCh37 |
| NC_000005.8:g.158940356C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_941139.1:n.2075+335C>G | ||
| XR_941140.1:n.2075+335C>G | ||
| XR_941141.1:n.570+335C>G | ||
| XR_941139.2:n.2229+335C>G |