Canonical Allele Identifier: CA62394227
Gene: ZNF804A HGNC NCBI

Linked Data

dbSNP Id: rs372046767
gnomAD v3: 2-184915477-G-C
gnomAD v4: 2-184915477-G-C
MyVariant Identifiers: chr2:g.185780204G>C (hg19) chr2:g.184915477G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.184915477G>C , CM000664.2:g.184915477G>C GRCh38
NC_000002.11:g.185780204G>C , CM000664.1:g.185780204G>C GRCh37
NC_000002.10:g.185488449G>C NCBI36
NG_046950.1:g.322112G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000302277.7:c.256-18126G>C MANE Select ENSP00000303252.6:n.256-18126G>C
ENST00000302277.6:c.256-18126G>C ENSP00000303252.6:n.256-18126G>C
ENST00000613975.1:c.1-18126G>C ENSP00000483032.1:n.1-18126G>C
NM_194250.1:c.256-18126G>C NP_919226.1:n.256-18126G>C
NM_194250.2:c.256-18126G>C MANE Select NP_919226.1:n.256-18126G>C
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