Canonical Allele Identifier:
CA2038655246
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.56983563C= , CM000674.2:g.56983563C= | GRCh38 |
| NC_000012.11:g.57377347C= , CM000674.1:g.57377347C= | GRCh37 |
| NC_000012.10:g.55663614C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000611536.1:n.530G= |