Canonical Allele Identifier:
CA2051430553
Gene:
Linked Data
dbSNP Id:
rs1272061051
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.84952227T>A , CM000674.2:g.84952227T>A | GRCh38 |
| NC_000012.11:g.85346006T>A , CM000674.1:g.85346006T>A | GRCh37 |
| NC_000012.10:g.83870137T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_945152.1:n.316+30913T>A | ||
| XR_945153.1:n.301+13763T>A | ||
| XR_945154.1:n.175-36715T>A | ||
| XR_945155.1:n.330+30913T>A | ||
| XR_945152.2:n.316+30913T>A | ||
| XR_945154.2:n.175-36715T>A | ||
| XR_945155.2:n.888+30913T>A |