Canonical Allele Identifier:
CA1929213466
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94762610T= , CM000672.2:g.94762610T= | GRCh38 |
| NC_000010.10:g.96522367T= , CM000672.1:g.96522367T= | GRCh37 |
| NC_000010.9:g.96512357T= | NCBI36 |
| NG_008384.2:g.4905T= | |
| NG_008384.3:g.4930T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000464755.1:c.932-12448T= | ENSP00000483243.1:n.932-12448T= |