Canonical Allele Identifier: CA62394182
Gene: ZNF804A HGNC NCBI

Linked Data

dbSNP Id: rs753792822
gnomAD v3: 2-184915095-T-G
gnomAD v4: 2-184915095-T-G
MyVariant Identifiers: chr2:g.185779822T>G (hg19) chr2:g.184915095T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.184915095T>G , CM000664.2:g.184915095T>G GRCh38
NC_000002.11:g.185779822T>G , CM000664.1:g.185779822T>G GRCh37
NC_000002.10:g.185488067T>G NCBI36
NG_046950.1:g.321730T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000302277.7:c.256-18508T>G MANE Select ENSP00000303252.6:n.256-18508T>G
ENST00000302277.6:c.256-18508T>G ENSP00000303252.6:n.256-18508T>G
ENST00000613975.1:c.1-18508T>G ENSP00000483032.1:n.1-18508T>G
NM_194250.1:c.256-18508T>G NP_919226.1:n.256-18508T>G
NM_194250.2:c.256-18508T>G MANE Select NP_919226.1:n.256-18508T>G
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