Canonical Allele Identifier:
CA180189147
Community Standard Title: NC_000008.11:g.78663569T>C
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.78663569T>C , CM000670.2:g.78663569T>C | GRCh38 |
| NC_000008.10:g.79575804T>C , CM000670.1:g.79575804T>C | GRCh37 |
| NC_000008.9:g.79738359T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_001745972.1:n.963+1436A>G | |
| XR_929074.1:n.975+1436A>G |