gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.22905778 (SAS)
Genomes Max Group AF
0.24913079 (SAS)
Exomes Max Group AF
0.22290875 (SAS)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.51964569G>A , CM000681.2:g.51964569G>A | GRCh38 |
| NC_000019.9:g.52467822G>A , CM000681.1:g.52467822G>A | GRCh37 |
| NC_000019.8:g.57159634G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000243644.9:c.*285C>T (ZNF350) MANE Select | ENSP00000243644.3:n.*285C>T | |
| ENST00000243644.8:c.*285C>T (ZNF350) | ENSP00000243644.3:n.*285C>T | |
| NM_021632.3:c.*285C>T (ZNF350) | NP_067645.3:n.*285C>T | |
| NR_103847.1:n.103-11822G>A (ZNF350-AS1) | ||
| XM_011527196.1:c.*285C>T (ZNF350) | XP_011525498.1:n.*285C>T | |
| XM_017027094.1:c.*285C>T (ZNF350) | XP_016882583.1:n.*285C>T | |
| XM_017027095.1:c.*285C>T (ZNF350) | XP_016882584.1:n.*285C>T | |
| XM_017027096.1:c.*285C>T (ZNF350) | XP_016882585.1:n.*285C>T | |
| XM_017027098.1:c.*285C>T (ZNF350) | XP_016882587.1:n.*285C>T | |
| XM_017027099.1:c.*285C>T (ZNF350) | XP_016882588.1:n.*285C>T | |
| XM_017027100.1:c.*285C>T (ZNF350) | XP_016882589.1:n.*285C>T | |
| XM_017027101.1:c.*285C>T (ZNF350) | XP_016882590.1:n.*285C>T | |
| XM_017027102.2:c.*285C>T (ZNF350) | XP_016882591.1:n.*285C>T | |
| XM_017027103.2:c.*285C>T (ZNF350) | XP_016882592.1:n.*285C>T | |
| XM_024451632.1:c.*285C>T (ZNF350) | XP_024307400.1:n.*285C>T | |
| XM_024451633.1:c.*285C>T (ZNF350) | XP_024307401.1:n.*285C>T | |
| XM_024451634.1:c.*285C>T (ZNF350) | XP_024307402.1:n.*285C>T | |
| XM_024451635.1:c.*285C>T (ZNF350) | XP_024307403.1:n.*285C>T | |
| NM_021632.4:c.*285C>T (ZNF350) MANE Select | NP_067645.3:n.*285C>T |