Canonical Allele Identifier:
CA2024154221
Gene:
Linked Data
dbSNP Id:
rs1865523509
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.28045182T>C , CM000674.2:g.28045182T>C | GRCh38 |
| NC_000012.11:g.28198115T>C , CM000674.1:g.28198115T>C | GRCh37 |
| NC_000012.10:g.28089382T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_931460.1:n.154-6224A>G |