dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.26774455C>A , CM000677.2:g.26774455C>A | GRCh38 |
| NC_000015.9:g.27019602C>A , CM000677.1:g.27019602C>A | GRCh37 |
| NC_000015.8:g.24570695C>A | NCBI36 |
| NG_012836.1:g.4326G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000541819.6:c.249-1683G>T | ENSP00000442408.2:n.249-1683G>T | |
| ENST00000557641.5:n.453-1683G>T |