Canonical Allele Identifier:
CA1644214072
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.86756774A= , CM000668.2:g.86756774A= | GRCh38 |
| NC_000006.11:g.87466492A= , CM000668.1:g.87466492A= | GRCh37 |
| NC_000006.10:g.87523211A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_942749.1:n.531-26531T= | ||
| XR_942750.1:n.511-26531T= |