Canonical Allele Identifier:
CA2788132295
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.57812851C>T , CM000672.2:g.57812851C>T | GRCh38 |
| NC_000010.10:g.59572611C>T , CM000672.1:g.59572611C>T | GRCh37 |
| NC_000010.9:g.59242617C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_945979.1:n.68+34441G>A | ||
| XR_001747454.1:n.85+34441G>A |