Canonical Allele Identifier:
CA214886253
Community Standard Title: NC_000010.11:g.121148705T>C
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.121148705T>C , CM000672.2:g.121148705T>C | GRCh38 |
| NC_000010.10:g.122908219T>C , CM000672.1:g.122908219T>C | GRCh37 |
| NC_000010.9:g.122898209T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_946379.1:n.286-3343T>C | |
| XR_946379.2:n.357-3343T>C |