Canonical Allele Identifier:
CA2255112059
Gene:
Linked Data
dbSNP Id:
rs1193762923
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.30237369T>A , CM000679.2:g.30237369T>A | GRCh38 |
| NC_000017.10:g.28564387T>A , CM000679.1:g.28564387T>A | GRCh37 |
| NC_000017.9:g.25588513T>A | NCBI36 |
| NG_011747.2:g.3568A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_934654.1:n.166-273T>A | ||
| XR_001752824.1:n.281-273T>A |