Canonical Allele Identifier:
CA1661878534
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.126643364A= , CM000668.2:g.126643364A= | GRCh38 |
| NC_000006.11:g.126964510A= , CM000668.1:g.126964510A= | GRCh37 |
| NC_000006.10:g.127006203A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650727.1:n.1167-21491T= | ||
| ENST00000651326.1:n.694-39899T= | ||
| ENST00000652545.1:n.1477-21491T= |