Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32112369A>C , CM000668.2:g.32112369A>C | GRCh38 |
| NC_000006.11:g.32080146A>C , CM000668.1:g.32080146A>C | GRCh37 |
| NC_000006.10:g.32188124A>C | NCBI36 |
| NG_008337.2:g.2006T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| ENST00000442721.1:c.-9+2625T>G (TNXB) | ENSP00000389946.1:n.-9+2625T>G |
| ENST00000494022.1:n.289+4335T>G (ATF6B) |