Canonical Allele Identifier:
CA2731473887
Gene:
Linked Data
dbSNP Id:
rs2141994972
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.87419309G>A , CM000677.2:g.87419309G>A | GRCh38 |
| NC_000015.9:g.87962540G>A , CM000677.1:g.87962540G>A | GRCh37 |
| NC_000015.8:g.85763544G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_932584.1:n.340-38C>T | ||
| XR_932585.1:n.340-38C>T | ||
| XR_001751647.1:n.617-38C>T | ||
| XR_932585.2:n.627-38C>T |