Canonical Allele Identifier:
CA2838418878
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.114399022G>A , CM000668.2:g.114399022G>A | GRCh38 |
| NC_000006.11:g.114720186G>A , CM000668.1:g.114720186G>A | GRCh37 |
| NC_000006.10:g.114826879G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_002956366.1:n.234+3741G>A | ||
| XR_002956367.1:n.234+3741G>A |