Linked Data
gnomAD v4:
12-12717357-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.12717357T>C , CM000674.2:g.12717357T>C | GRCh38 |
| NC_000012.11:g.12870291T>C , CM000674.1:g.12870291T>C | GRCh37 |
| NC_000012.10:g.12761558T>C | NCBI36 |
| NG_016341.1:g.4990T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682620.1:n.1631-1468T>C (CDKN1B) | ||
| ENST00000684771.1:n.585-1468T>C (CDKN1B) | ||
| ENST00000228872.8:c.-483T>C (CDKN1B) | ENSP00000228872.4:n.-483T>C | |
| ENST00000477087.1:n.155-1468T>C (CDKN1B) | ||
| NM_004064.4:c.-483T>C (CDKN1B) | NP_004055.1:n.-483T>C | |
| XM_011520623.3:c.-1851A>G (GPR19) | XP_011518925.1:n.-1851A>G | |
| XM_017019216.2:c.-1879A>G (GPR19) | XP_016874705.1:n.-1879A>G |