Canonical Allele Identifier:
CA1552561735
Gene:
Linked Data
dbSNP Id:
rs10069397
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.66487881T>A , CM000667.2:g.66487881T>A | GRCh38 |
| NC_000005.9:g.65783709T>A , CM000667.1:g.65783709T>A | GRCh37 |
| NC_000005.8:g.65819465T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_948381.1:n.649-48955T>A |