Linked Data
dbSNP Id:
rs17638629
gnomAD v2:
19-12225372-T-G
gnomAD v3:
19-12114557-T-G
gnomAD v4:
19-12114557-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.12114557T>G , CM000681.2:g.12114557T>G | GRCh38 |
| NC_000019.9:g.12225372T>G , CM000681.1:g.12225372T>G | GRCh37 |
| NC_000019.8:g.12086372T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000430298.6:c.*3253T>G (ZNF788P) | ENSP00000391703.1:n.*3253T>G | |
| ENST00000600335.5:c.191+20943A>C (ZNF20) | ENSP00000470025.1:n.191+20943A>C | |
| ENST00000601686.1:n.165-21218T>G (ZNF788P) | ||
| NR_027049.1:n.3647T>G (ZNF788P) | ||
| NM_001348163.1:c.*1162T>G (ZNF788P) | NP_001335092.1:n.*1162T>G | |
| NM_001348164.1:c.*1162T>G (ZNF788P) | NP_001335093.1:n.*1162T>G | |
| NM_001348165.1:c.*1162T>G (ZNF788P) | NP_001335094.1:n.*1162T>G | |
| XM_024451502.1:c.*1162T>G (ZNF788P) | XP_024307270.1:n.*1162T>G | |
| NM_001348163.2:c.*1162T>G (ZNF788P) | NP_001335092.1:n.*1162T>G | |
| NM_001348164.2:c.*1162T>G (ZNF788P) | NP_001335093.1:n.*1162T>G | |
| NM_001348165.2:c.*1162T>G (ZNF788P) | NP_001335094.1:n.*1162T>G | |
| NR_171037.1:n.3673T>G (ZNF788P) | ||
| NR_171038.1:n.3486T>G (ZNF788P) | ||
| NR_171039.1:n.3613T>G (ZNF788P) | ||
| NR_171040.1:n.3734T>G (ZNF788P) | ||
| NR_171041.1:n.3607T>G (ZNF788P) | ||
| NR_171042.1:n.3547T>G (ZNF788P) | ||
| NR_171043.1:n.3674T>G (ZNF788P) |