Canonical Allele Identifier:
CA2697564126
Gene:
Linked Data
dbSNP Id:
rs1336887776
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.193121777T>G , CM000663.2:g.193121777T>G | GRCh38 |
| NC_000001.10:g.193090907T>G , CM000663.1:g.193090907T>G | GRCh37 |
| NC_000001.9:g.191357530T>G | NCBI36 |
| NG_012691.1:g.4820T>G , LRG_507:g.4820T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001738350.1:n.1880A>C |