Canonical Allele Identifier:
CA1374121547
Gene:
Linked Data
dbSNP Id:
rs1704106513
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.72266757T>C , CM000665.2:g.72266757T>C | GRCh38 |
| NC_000003.11:g.72315908T>C , CM000665.1:g.72315908T>C | GRCh37 |
| NC_000003.10:g.72398598T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_940958.1:n.835+8351A>G |