Canonical Allele Identifier:
CA2246165978
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8137792G= , CM000679.2:g.8137792G= | GRCh38 |
| NC_000017.10:g.8041110G= , CM000679.1:g.8041110G= | GRCh37 |
| NC_000017.9:g.7981835G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_934202.1:n.183-1057G= | ||
| XR_934203.1:n.70-1685G= | ||
| XR_934202.2:n.414-1057G= |