Canonical Allele Identifier:
CA1439212869
Gene:
Linked Data
dbSNP Id:
rs1711589837
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.12578242T>C , CM000666.2:g.12578242T>C | GRCh38 |
| NC_000004.11:g.12579866T>C , CM000666.1:g.12579866T>C | GRCh37 |
| NC_000004.10:g.12188964T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_925406.1:n.106+31100A>G | ||
| XR_001741374.1:n.254+44413A>G | ||
| XR_925406.3:n.140+31100A>G |