Canonical Allele Identifier:
CA2581796136
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.176127051A>T , CM000664.2:g.176127051A>T | GRCh38 |
| NC_000002.11:g.176991779A>T , CM000664.1:g.176991779A>T | GRCh37 |
| NC_000002.10:g.176700025A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_241351.3:n.2581T>A |