Canonical Allele Identifier:
CA2024154226
Gene:
Linked Data
dbSNP Id:
rs1865523570
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.28045193G>C , CM000674.2:g.28045193G>C | GRCh38 |
| NC_000012.11:g.28198126G>C , CM000674.1:g.28198126G>C | GRCh37 |
| NC_000012.10:g.28089393G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_931460.1:n.154-6235C>G |