Canonical Allele Identifier:
CA12996538
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.108110027C>T , CM000671.2:g.108110027C>T | GRCh38 |
| NC_000009.11:g.110872307C>T , CM000671.1:g.110872307C>T | GRCh37 |
| NC_000009.10:g.109912128C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930239.1:n.461-56733G>A | ||
| XR_001746881.1:n.668-56733G>A | ||
| XR_001746882.1:n.668-56733G>A |