Canonical Allele Identifier:
CA2560380695
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.122884126T>C , CM000664.2:g.122884126T>C | GRCh38 |
| NC_000002.11:g.123641702T>C , CM000664.1:g.123641702T>C | GRCh37 |
| NC_000002.10:g.123358172T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923292.1:n.1125-816T>C | ||
| XR_001739692.1:n.1451-816T>C | ||
| XR_923292.2:n.1358-816T>C |