Canonical Allele Identifier:
CA2751871529
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.118079674C>T , CM000664.2:g.118079674C>T | GRCh38 |
| NC_000002.11:g.118837250C>T , CM000664.1:g.118837250C>T | GRCh37 |
| NC_000002.10:g.118553720C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011512305.1:c.697-2142G>A | XP_011510607.1:n.697-2142G>A | |
| XR_001739662.2:n.138+8577G>A |