Canonical Allele Identifier:
CA2838462788
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.26609399T>A , CM000669.2:g.26609399T>A | GRCh38 |
| NC_000007.13:g.26649018T>A , CM000669.1:g.26649018T>A | GRCh37 |
| NC_000007.12:g.26615543T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_927131.1:n.1117+7849A>T | ||
| XR_927131.2:n.1185+7849A>T |