Linked Data
dbSNP Id:
rs1404212831
gnomAD v2:
12-12870588-G-T
gnomAD v3:
12-12717654-G-T
gnomAD v4:
12-12717654-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.12717654G>T , CM000674.2:g.12717654G>T | GRCh38 |
| NC_000012.11:g.12870588G>T , CM000674.1:g.12870588G>T | GRCh37 |
| NC_000012.10:g.12761855G>T | NCBI36 |
| NG_016341.1:g.5287G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614874.2:c.-186G>T (CDKN1B) | ENSP00000507272.1:n.-186G>T | |
| ENST00000682620.1:n.1631-1171G>T (CDKN1B) | ||
| ENST00000684771.1:n.585-1171G>T (CDKN1B) | ||
| ENST00000228872.9:c.-186G>T (CDKN1B) MANE Select | ENSP00000228872.4:n.-186G>T | |
| ENST00000228872.8:c.-186G>T (CDKN1B) | ENSP00000228872.4:n.-186G>T | |
| ENST00000477087.1:n.155-1171G>T (CDKN1B) | ||
| NM_004064.4:c.-186G>T (CDKN1B) | NP_004055.1:n.-186G>T | |
| XM_011520623.3:c.-2148C>A (GPR19) | XP_011518925.1:n.-2148C>A | |
| XM_017019216.2:c.-2176C>A (GPR19) | XP_016874705.1:n.-2176C>A | |
| NM_004064.5:c.-186G>T (CDKN1B) MANE Select | NP_004055.1:n.-186G>T |