Canonical Allele Identifier:
CA2697596673
Gene:
Linked Data
dbSNP Id:
rs1675452571
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.193121933C>A , CM000663.2:g.193121933C>A | GRCh38 |
| NC_000001.10:g.193091063C>A , CM000663.1:g.193091063C>A | GRCh37 |
| NC_000001.9:g.191357686C>A | NCBI36 |
| NG_012691.1:g.4976C>A , LRG_507:g.4976C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001738350.1:n.1724G>T |