Canonical Allele Identifier:
CA2263926980
Gene:
Linked Data
dbSNP Id:
rs1908570969
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.50211854A>T , CM000679.2:g.50211854A>T | GRCh38 |
| NC_000017.10:g.48289215A>T , CM000679.1:g.48289215A>T | GRCh37 |
| NC_000017.9:g.45644214A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_934838.1:n.43-1981A>T |