Canonical Allele Identifier:
CA1419898219
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.170412314C= , CM000665.2:g.170412314C= | GRCh38 |
| NC_000003.11:g.170130102C= , CM000665.1:g.170130102C= | GRCh37 |
| NC_000003.10:g.171612796C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_924700.1:n.238-483C= |