Canonical Allele Identifier:
CA1284674318
Gene:
Linked Data
dbSNP Id:
rs1573479130
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.122884149T>G , CM000664.2:g.122884149T>G | GRCh38 |
| NC_000002.11:g.123641725T>G , CM000664.1:g.123641725T>G | GRCh37 |
| NC_000002.10:g.123358195T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923292.1:n.1125-793T>G | ||
| XR_001739692.1:n.1451-793T>G | ||
| XR_923292.2:n.1358-793T>G |