dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32407575A>T , CM000668.2:g.32407575A>T | GRCh38 |
| NC_000006.11:g.32375352A>T , CM000668.1:g.32375352A>T | GRCh37 |
| NC_000006.10:g.32483330A>T | NCBI36 |
| NG_054759.1:g.6305T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011514755.1:c.-452T>A (BTNL2) | XP_011513057.1:n.-452T>A | |
| XM_011514756.1:c.-452T>A (BTNL2) | XP_011513058.1:n.-452T>A | |
| XM_011515039.1:c.*1444A>T (TSBP1-AS1) | XP_011513341.1:n.*1444A>T | |
| XR_926699.1:n.1666A>T (TSBP1-AS1) | ||
| NR_136245.1:n.1865A>T (TSBP1-AS1) | ||
| XM_017011057.1:c.-452T>A (BTNL2) | XP_016866546.1:n.-452T>A |