Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.12717318C>G , CM000674.2:g.12717318C>G | GRCh38 |
| NC_000012.11:g.12870252C>G , CM000674.1:g.12870252C>G | GRCh37 |
| NC_000012.10:g.12761519C>G | NCBI36 |
| NG_016341.1:g.4951C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682620.1:n.1631-1507C>G (CDKN1B) | ||
| ENST00000684771.1:n.585-1507C>G (CDKN1B) | ||
| ENST00000228872.8:c.-522C>G (CDKN1B) | ENSP00000228872.4:n.-522C>G | |
| ENST00000477087.1:n.154+1435C>G (CDKN1B) | ||
| NM_004064.4:c.-522C>G (CDKN1B) | NP_004055.1:n.-522C>G | |
| XM_011520623.3:c.-1812G>C (GPR19) | XP_011518925.1:n.-1812G>C | |
| XM_017019216.2:c.-1840G>C (GPR19) | XP_016874705.1:n.-1840G>C |