Canonical Allele Identifier:
CA1284674129
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.122883972G= , CM000664.2:g.122883972G= | GRCh38 |
| NC_000002.11:g.123641548G= , CM000664.1:g.123641548G= | GRCh37 |
| NC_000002.10:g.123358018G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923292.1:n.1125-970G= | ||
| XR_001739692.1:n.1451-970G= | ||
| XR_923292.2:n.1358-970G= |