Linked Data
dbSNP Id:
rs973773605
gnomAD v2:
12-12870376-T-C
gnomAD v3:
12-12717442-T-C
gnomAD v4:
12-12717442-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.12717442T>C , CM000674.2:g.12717442T>C | GRCh38 |
| NC_000012.11:g.12870376T>C , CM000674.1:g.12870376T>C | GRCh37 |
| NC_000012.10:g.12761643T>C | NCBI36 |
| NG_016341.1:g.5075T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614874.2:c.-398T>C (CDKN1B) | ENSP00000507272.1:n.-398T>C | |
| ENST00000682620.1:n.1631-1383T>C (CDKN1B) | ||
| ENST00000684771.1:n.585-1383T>C (CDKN1B) | ||
| ENST00000228872.9:c.-398T>C (CDKN1B) MANE Select | ENSP00000228872.4:n.-398T>C | |
| ENST00000228872.8:c.-398T>C (CDKN1B) | ENSP00000228872.4:n.-398T>C | |
| ENST00000477087.1:n.155-1383T>C (CDKN1B) | ||
| NM_004064.4:c.-398T>C (CDKN1B) | NP_004055.1:n.-398T>C | |
| XM_011520623.3:c.-1936A>G (GPR19) | XP_011518925.1:n.-1936A>G | |
| XM_017019216.2:c.-1964A>G (GPR19) | XP_016874705.1:n.-1964A>G | |
| NM_004064.5:c.-398T>C (CDKN1B) MANE Select | NP_004055.1:n.-398T>C |