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