Canonical Allele Identifier:
CA1369169850
Gene:
Linked Data
dbSNP Id:
rs2041752938
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.61428080A>T , CM000665.2:g.61428080A>T | GRCh38 |
| NC_000003.11:g.61413754A>T , CM000665.1:g.61413754A>T | GRCh37 |
| NC_000003.10:g.61388794A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_940892.1:n.165-394T>A | ||
| XR_940893.1:n.164+434T>A | ||
| XR_001740725.1:n.202+434T>A | ||
| XR_940892.2:n.203-394T>A |