Canonical Allele Identifier: CA15212499
Gene: ZNF804A HGNC NCBI
MyVariant.info:
GRCh38 chr2:g.184902089A>G
GRCh37 chr2:g.185766816A>G
gnomAD v2:
2:185766816 A / G
gnomAD v3:
2:184902089 A / G
gnomAD v4:
chr2-184902089-A-G
Joint Max Group AF 0.79880741 (EAS)
Genomes Max Group AF 0.79858787 (EAS)
Exomes Max Group AF 0.45376388 (NFE)
dbSNP:
7603001
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.184902089A>G , CM000664.2:g.184902089A>G GRCh38
NC_000002.11:g.185766816A>G , CM000664.1:g.185766816A>G GRCh37
NC_000002.10:g.185475061A>G NCBI36
NG_046950.1:g.308724A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000302277.7:c.256-31514A>G MANE Select ENSP00000303252.6:n.256-31514A>G
ENST00000302277.6:c.256-31514A>G ENSP00000303252.6:n.256-31514A>G
ENST00000613975.1:c.1-31514A>G ENSP00000483032.1:n.1-31514A>G
NM_194250.1:c.256-31514A>G NP_919226.1:n.256-31514A>G
NM_194250.2:c.256-31514A>G MANE Select NP_919226.1:n.256-31514A>G
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