Linked Data
dbSNP Id:
rs1015676062
gnomAD v2:
12-12870212-G-A
gnomAD v3:
12-12717278-G-A
gnomAD v4:
12-12717278-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.12717278G>A , CM000674.2:g.12717278G>A | GRCh38 |
| NC_000012.11:g.12870212G>A , CM000674.1:g.12870212G>A | GRCh37 |
| NC_000012.10:g.12761479G>A | NCBI36 |
| NG_016341.1:g.4911G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682620.1:n.1631-1547G>A (CDKN1B) | ||
| ENST00000684771.1:n.585-1547G>A (CDKN1B) | ||
| ENST00000228872.8:c.-562G>A (CDKN1B) | ENSP00000228872.4:n.-562G>A | |
| ENST00000477087.1:n.154+1395G>A (CDKN1B) | ||
| NM_004064.4:c.-562G>A (CDKN1B) | NP_004055.1:n.-562G>A | |
| XM_011520623.3:c.-1772C>T (GPR19) | XP_011518925.1:n.-1772C>T | |
| XM_017019216.2:c.-1800C>T (GPR19) | XP_016874705.1:n.-1800C>T |