Canonical Allele Identifier:
CA1282456429
Gene:
Linked Data
dbSNP Id:
rs1678006942
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.118079620G>C , CM000664.2:g.118079620G>C | GRCh38 |
| NC_000002.11:g.118837196G>C , CM000664.1:g.118837196G>C | GRCh37 |
| NC_000002.10:g.118553666G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011512305.1:c.697-2088C>G | XP_011510607.1:n.697-2088C>G | |
| XR_001739662.2:n.138+8631C>G |