Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.12717322T>A , CM000674.2:g.12717322T>A | GRCh38 |
| NC_000012.11:g.12870256T>A , CM000674.1:g.12870256T>A | GRCh37 |
| NC_000012.10:g.12761523T>A | NCBI36 |
| NG_016341.1:g.4955T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682620.1:n.1631-1503T>A (CDKN1B) | ||
| ENST00000684771.1:n.585-1503T>A (CDKN1B) | ||
| ENST00000228872.8:c.-518T>A (CDKN1B) | ENSP00000228872.4:n.-518T>A | |
| ENST00000477087.1:n.154+1439T>A (CDKN1B) | ||
| NM_004064.4:c.-518T>A (CDKN1B) | NP_004055.1:n.-518T>A | |
| XM_011520623.3:c.-1816A>T (GPR19) | XP_011518925.1:n.-1816A>T | |
| XM_017019216.2:c.-1844A>T (GPR19) | XP_016874705.1:n.-1844A>T |