Canonical Allele Identifier:
CA1369169849
Gene:
Linked Data
dbSNP Id:
rs2041752928
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.61428074G>C , CM000665.2:g.61428074G>C | GRCh38 |
| NC_000003.11:g.61413748G>C , CM000665.1:g.61413748G>C | GRCh37 |
| NC_000003.10:g.61388788G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_940892.1:n.165-388C>G | ||
| XR_940893.1:n.164+440C>G | ||
| XR_001740725.1:n.202+440C>G | ||
| XR_940892.2:n.203-388C>G |