Canonical Allele Identifier:
CA11309486
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.74712049T>C , CM000664.2:g.74712049T>C | GRCh38 |
| NC_000002.11:g.74939176T>C , CM000664.1:g.74939176T>C | GRCh37 |
| NC_000002.10:g.74792684T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_427047.4:n.362T>C |