Canonical Allele Identifier:
CA860876686
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.134540402G>C , CM000671.2:g.134540402G>C | GRCh38 |
| NC_000009.11:g.137432248G>C , CM000671.1:g.137432248G>C | GRCh37 |
| NC_000009.10:g.136572069G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_109854.3:n.2568-4518G>C | ||
| XR_930416.1:n.171-4518G>C | ||
| XR_930417.1:n.342-4518G>C | ||
| XR_109854.5:n.2497-4518G>C | ||
| XR_930416.2:n.194-4518G>C | ||
| XR_930417.2:n.365-4518G>C |