dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.12715152G>T , CM000674.2:g.12715152G>T | GRCh38 |
| NC_000012.11:g.12868086G>T , CM000674.1:g.12868086G>T | GRCh37 |
| NC_000012.10:g.12759353G>T | NCBI36 |
| NG_016341.1:g.2785G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682080.1:n.2305G>T (CDKN1B) | ||
| ENST00000682620.1:n.1631-3673G>T (CDKN1B) | ||
| ENST00000684771.1:n.585-3673G>T (CDKN1B) | ||
| ENST00000477087.1:n.47+48G>T (CDKN1B) | ||
| XM_011520623.1:c.-205+559C>A (GPR19) | XP_011518925.1:n.-205+559C>A | |
| XM_011520623.3:c.-205+559C>A (GPR19) | XP_011518925.1:n.-205+559C>A | |
| XM_017019216.2:c.-233+559C>A (GPR19) | XP_016874705.1:n.-233+559C>A |