gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.18585896 (AMR)
Genomes Max Group AF
0.18585896 (AMR)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.58580292A>G , CM000673.2:g.58580292A>G | GRCh38 |
| NC_000011.9:g.58347765A>G , CM000673.1:g.58347765A>G | GRCh37 |
| NC_000011.8:g.58104341A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000316059.7:c.341+670A>G (ZFP91) MANE Select | ENSP00000339030.5:n.341+670A>G | |
| ENST00000316059.6:c.341+670A>G (ZFP91) | ENSP00000339030.5:n.341+670A>G | |
| ENST00000389919.8:c.341+670A>G (ZFP91-CNTF) | ENSP00000455911.1:n.341+670A>G | |
| NM_001197051.1:c.341+670A>G (ZFP91) | NP_001183980.1:n.341+670A>G | |
| NM_053023.4:c.341+670A>G (ZFP91) | NP_444251.1:n.341+670A>G | |
| NR_024091.1:n.509+670A>G (ZFP91-CNTF) | ||
| NM_053023.5:c.341+670A>G (ZFP91) MANE Select | NP_444251.1:n.341+670A>G | |
| NM_001197051.2:c.341+670A>G (ZFP91) | NP_001183980.1:n.341+670A>G |