Canonical Allele Identifier:
CA2733483847
Gene:
Linked Data
dbSNP Id:
rs2143017448
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.30237417G>T , CM000679.2:g.30237417G>T | GRCh38 |
| NC_000017.10:g.28564435G>T , CM000679.1:g.28564435G>T | GRCh37 |
| NC_000017.9:g.25588561G>T | NCBI36 |
| NG_011747.2:g.3520C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_934654.1:n.166-225G>T | ||
| XR_001752824.1:n.281-225G>T |