Canonical Allele Identifier:
CA2815053038
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.2471002C>G , CM000682.2:g.2471002C>G | GRCh38 |
| NC_000020.10:g.2451648C>G , CM000682.1:g.2451648C>G | GRCh37 |
| NC_000020.9:g.2399648C>G | NCBI36 |
| NG_042057.1:g.4852G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461548.1:c.305-3244G>C | ENSP00000456213.1:n.305-3244G>C |