Canonical Allele Identifier:
CA12176438
Community Standard Title: NC_000006.12:g.475489C>T
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.475489C>T , CM000668.2:g.475489C>T | GRCh38 |
| NC_000006.11:g.475489C>T , CM000668.1:g.475489C>T | GRCh37 |
| NC_000006.10:g.420489C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_001743914.1:n.763C>T | |
| XR_926364.1:n.2715-9204C>T | |
| XR_926365.1:n.2549-9204C>T |