Canonical Allele Identifier:
CA2510221338
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.66487916C>T , CM000667.2:g.66487916C>T | GRCh38 |
| NC_000005.9:g.65783744C>T , CM000667.1:g.65783744C>T | GRCh37 |
| NC_000005.8:g.65819500C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_948381.1:n.649-48920C>T |