Canonical Allele Identifier:
CA1929213246
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94762423G= , CM000672.2:g.94762423G= | GRCh38 |
| NC_000010.10:g.96522180G= , CM000672.1:g.96522180G= | GRCh37 |
| NC_000010.9:g.96512170G= | NCBI36 |
| NG_008384.2:g.4718G= | |
| NG_008384.3:g.4743G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000464755.1:c.932-12635G= | ENSP00000483243.1:n.932-12635G= |