Linked Data
gnomAD v4:
12-12717271-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.12717271T>G , CM000674.2:g.12717271T>G | GRCh38 |
| NC_000012.11:g.12870205T>G , CM000674.1:g.12870205T>G | GRCh37 |
| NC_000012.10:g.12761472T>G | NCBI36 |
| NG_016341.1:g.4904T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682620.1:n.1631-1554T>G (CDKN1B) | ||
| ENST00000684771.1:n.585-1554T>G (CDKN1B) | ||
| ENST00000228872.8:c.-569T>G (CDKN1B) | ENSP00000228872.4:n.-569T>G | |
| ENST00000477087.1:n.154+1388T>G (CDKN1B) | ||
| NM_004064.4:c.-569T>G (CDKN1B) | NP_004055.1:n.-569T>G | |
| XM_011520623.1:c.-1765A>C (GPR19) | XP_011518925.1:n.-1765A>C | |
| XM_011520623.3:c.-1765A>C (GPR19) | XP_011518925.1:n.-1765A>C | |
| XM_017019216.2:c.-1793A>C (GPR19) | XP_016874705.1:n.-1793A>C |