Canonical Allele Identifier:
CA1672979349
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.151633794C= , CM000668.2:g.151633794C= | GRCh38 |
| NC_000006.11:g.151954929C= , CM000668.1:g.151954929C= | GRCh37 |
| NC_000006.10:g.151996622C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943115.1:n.2496+3812C= |