Canonical Allele Identifier:
CA1350284107
Gene:
Linked Data
dbSNP Id:
rs945021129
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.21207198T>C , CM000665.2:g.21207198T>C | GRCh38 |
| NC_000003.11:g.21248690T>C , CM000665.1:g.21248690T>C | GRCh37 |
| NC_000003.10:g.21223694T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_940646.1:n.254-3800T>C | ||
| XR_940646.2:n.547-3800T>C |