Canonical Allele Identifier:
CA1502607421
Gene:
Linked Data
dbSNP Id:
rs1732906167
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.148748461C>T , CM000666.2:g.148748461C>T | GRCh38 |
| NC_000004.11:g.149669613C>T , CM000666.1:g.149669613C>T | GRCh37 |
| NC_000004.10:g.149889063C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001741441.1:n.1746-118296C>T |