Canonical Allele Identifier:
CA2112050601
Gene:
Linked Data
dbSNP Id:
rs1878600137
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.94853056T>G , CM000675.2:g.94853056T>G | GRCh38 |
| NC_000013.10:g.95505310T>G , CM000675.1:g.95505310T>G | GRCh37 |
| NC_000013.9:g.94303311T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_110754.1:n.257-52408T>G |