Canonical Allele Identifier:
CA2193710488
Gene:
Linked Data
dbSNP Id:
rs1895002131
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.87419433G>A , CM000677.2:g.87419433G>A | GRCh38 |
| NC_000015.9:g.87962664G>A , CM000677.1:g.87962664G>A | GRCh37 |
| NC_000015.8:g.85763668G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_932584.1:n.340-162C>T | ||
| XR_932585.1:n.340-162C>T | ||
| XR_001751647.1:n.617-162C>T | ||
| XR_932585.2:n.627-162C>T |