Canonical Allele Identifier:
CA1374121677
Gene:
Linked Data
dbSNP Id:
rs1704109297
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.72266915G>A , CM000665.2:g.72266915G>A | GRCh38 |
| NC_000003.11:g.72316066G>A , CM000665.1:g.72316066G>A | GRCh37 |
| NC_000003.10:g.72398756G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_940958.1:n.835+8193C>T |