Linked Data
dbSNP Id:
rs1946471291
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.12717281C>G , CM000674.2:g.12717281C>G | GRCh38 |
| NC_000012.11:g.12870215C>G , CM000674.1:g.12870215C>G | GRCh37 |
| NC_000012.10:g.12761482C>G | NCBI36 |
| NG_016341.1:g.4914C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682620.1:n.1631-1544C>G (CDKN1B) | ||
| ENST00000684771.1:n.585-1544C>G (CDKN1B) | ||
| ENST00000228872.8:c.-559C>G (CDKN1B) | ENSP00000228872.4:n.-559C>G | |
| ENST00000477087.1:n.154+1398C>G (CDKN1B) | ||
| NM_004064.4:c.-559C>G (CDKN1B) | NP_004055.1:n.-559C>G | |
| XM_011520623.3:c.-1775G>C (GPR19) | XP_011518925.1:n.-1775G>C | |
| XM_017019216.2:c.-1803G>C (GPR19) | XP_016874705.1:n.-1803G>C |