Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.12717262G= , CM000674.2:g.12717262G= | GRCh38 |
| NC_000012.11:g.12870196G= , CM000674.1:g.12870196G= | GRCh37 |
| NC_000012.10:g.12761463G= | NCBI36 |
| NG_016341.1:g.4895G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682620.1:n.1631-1563G= (CDKN1B) | ||
| ENST00000684771.1:n.585-1563G= (CDKN1B) | ||
| ENST00000228872.8:c.-578G= (CDKN1B) | ENSP00000228872.4:n.-578G= | |
| ENST00000477087.1:n.154+1379G= (CDKN1B) | ||
| XM_011520623.1:c.-1756C= (GPR19) | XP_011518925.1:n.-1756C= | |
| XM_011520623.3:c.-1756C= (GPR19) | XP_011518925.1:n.-1756C= | |
| XM_017019216.2:c.-1784C= (GPR19) | XP_016874705.1:n.-1784C= |