Canonical Allele Identifier:
CA1365145662
Gene:
Linked Data
dbSNP Id:
rs1559566534
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.53057094G>A , CM000665.2:g.53057094G>A | GRCh38 |
| NC_000003.11:g.53091110G>A , CM000665.1:g.53091110G>A | GRCh37 |
| NC_000003.10:g.53066150G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000607203.1:c.318-9855C>T | ||
| ENST00000607283.5:c.465-13840C>T | ||
| ENST00000607495.5:c.447+20594C>T |