Canonical Allele Identifier: CA538374860
Gene: ZNF804A HGNC NCBI

Linked Data

dbSNP Id: rs1450050434
gnomAD v2: 2-185780392-A-G
gnomAD v3: 2-184915665-A-G
gnomAD v4: 2-184915665-A-G
MyVariant Identifiers: chr2:g.185780392A>G (hg19) chr2:g.184915665A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.184915665A>G , CM000664.2:g.184915665A>G GRCh38
NC_000002.11:g.185780392A>G , CM000664.1:g.185780392A>G GRCh37
NC_000002.10:g.185488637A>G NCBI36
NG_046950.1:g.322300A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000302277.7:c.256-17938A>G MANE Select ENSP00000303252.6:n.256-17938A>G
ENST00000302277.6:c.256-17938A>G ENSP00000303252.6:n.256-17938A>G
ENST00000613975.1:c.1-17938A>G ENSP00000483032.1:n.1-17938A>G
NM_194250.1:c.256-17938A>G NP_919226.1:n.256-17938A>G
NM_194250.2:c.256-17938A>G MANE Select NP_919226.1:n.256-17938A>G
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