Canonical Allele Identifier:
CA1439212498
Gene:
Linked Data
dbSNP Id:
rs1711566650
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.12577868A>G , CM000666.2:g.12577868A>G | GRCh38 |
| NC_000004.11:g.12579492A>G , CM000666.1:g.12579492A>G | GRCh37 |
| NC_000004.10:g.12188590A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_925406.1:n.106+31474T>C | ||
| XR_001741374.1:n.254+44787T>C | ||
| XR_925406.3:n.140+31474T>C |