Canonical Allele Identifier:
CA2697526113
Gene:
Linked Data
dbSNP Id:
rs747241730
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.193121766T>A , CM000663.2:g.193121766T>A | GRCh38 |
| NC_000001.10:g.193090896T>A , CM000663.1:g.193090896T>A | GRCh37 |
| NC_000001.9:g.191357519T>A | NCBI36 |
| NG_012691.1:g.4809T>A , LRG_507:g.4809T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001738350.1:n.1891A>T |