Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32289532G>C , CM000668.2:g.32289532G>C | GRCh38 |
| NC_000006.11:g.32257309G>C , CM000668.1:g.32257309G>C | GRCh37 |
| NC_000006.10:g.32365287G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000442822.6:c.1360-863C>G (TSBP1) | ENSP00000411164.2:n.1360-863C>G | |
| XM_011514236.1:c.*1487-606C>G (TSBP1) | XP_011512538.1:n.*1487-606C>G | |
| XM_011515039.1:c.421+26723G>C (TSBP1-AS1) | XP_011513341.1:n.421+26723G>C | |
| XM_011515040.1:c.421+26723G>C (TSBP1-AS1) | XP_011513342.1:n.421+26723G>C | |
| NR_136244.1:n.440+26723G>C (TSBP1-AS1) | ||
| NR_136245.1:n.242+34118G>C (TSBP1-AS1) | ||
| NR_136246.1:n.242+34118G>C (TSBP1-AS1) |