Canonical Allele Identifier:
CA1374121671
Gene:
Linked Data
dbSNP Id:
rs1704109242
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.72266908C>T , CM000665.2:g.72266908C>T | GRCh38 |
| NC_000003.11:g.72316059C>T , CM000665.1:g.72316059C>T | GRCh37 |
| NC_000003.10:g.72398749C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_940958.1:n.835+8200G>A |