dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.45448194G>T , CM000677.2:g.45448194G>T | GRCh38 |
| NC_000015.9:g.45740392G>T , CM000677.1:g.45740392G>T | GRCh37 |
| NC_000015.8:g.43527684G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000558435.5:c.184-355G>T (C15orf48) | ENSP00000452967.1:n.184-355G>T | |
| XM_017022774.1:c.166-124G>T (SLC30A4-AS1) | XP_016878263.1:n.166-124G>T |