Canonical Allele Identifier:
CA2568718439
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.195007059C>G , CM000664.2:g.195007059C>G | GRCh38 |
| NC_000002.11:g.195871783C>G , CM000664.1:g.195871783C>G | GRCh37 |
| NC_000002.10:g.195580028C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_001739836.1:n.553+52376G>C |