Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.17148802A>C , CM000667.2:g.17148802A>C | GRCh38 |
| NC_000005.9:g.17148911A>C , CM000667.1:g.17148911A>C | GRCh37 |
| NC_000005.8:g.17201911A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NR_027253.1:n.1443+13667T>G (BASP1-AS1) | |
| ENST00000606445.1:c.-73+59641A>C (BASP1) | ENSP00000476090.1:n.-73+59641A>C |