Canonical Allele Identifier: CA761931090
Gene: ZNF804A HGNC NCBI

Linked Data

dbSNP Id: rs1438927077
gnomAD v3: 2-184913937-G-A
gnomAD v4: 2-184913937-G-A
MyVariant Identifiers: chr2:g.185778664G>A (hg19) chr2:g.184913937G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.184913937G>A , CM000664.2:g.184913937G>A GRCh38
NC_000002.11:g.185778664G>A , CM000664.1:g.185778664G>A GRCh37
NC_000002.10:g.185486909G>A NCBI36
NG_046950.1:g.320572G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000302277.7:c.256-19666G>A MANE Select ENSP00000303252.6:n.256-19666G>A
ENST00000302277.6:c.256-19666G>A ENSP00000303252.6:n.256-19666G>A
ENST00000613975.1:c.1-19666G>A ENSP00000483032.1:n.1-19666G>A
NM_194250.1:c.256-19666G>A NP_919226.1:n.256-19666G>A
NM_194250.2:c.256-19666G>A MANE Select NP_919226.1:n.256-19666G>A
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