Canonical Allele Identifier:
CA12442695
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.41761668T>C , CM000668.2:g.41761668T>C | GRCh38 |
| NC_000006.11:g.41729406T>C , CM000668.1:g.41729406T>C | GRCh37 |
| NC_000006.10:g.41837384T>C | NCBI36 |