Canonical Allele Identifier:
CA7910040
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.13920136T>A , CM000678.2:g.13920136T>A | GRCh38 |
| NC_000016.9:g.14013993T>A , CM000678.1:g.14013993T>A | GRCh37 |
| NC_000016.8:g.13921494T>A | NCBI36 |
| NG_011442.1:g.4980T>A , LRG_463:g.4980T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_933098.1:n.82+6389A>T | |
| XR_933099.1:n.82+6389A>T | |
| XR_933100.1:n.82+6389A>T |