Canonical Allele Identifier:
CA1264999444
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.81645798C= , CM000664.2:g.81645798C= | GRCh38 |
| NC_000002.11:g.81872922C= , CM000664.1:g.81872922C= | GRCh37 |
| NC_000002.10:g.81726433C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_940294.1:n.563+66189C= | ||
| XR_940295.1:n.485+97051C= | ||
| XR_001739571.1:n.485+97051C= |