Canonical Allele Identifier: CA1313504170
Gene: ZNF804A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.184915109G= , CM000664.2:g.184915109G= GRCh38
NC_000002.11:g.185779836G= , CM000664.1:g.185779836G= GRCh37
NC_000002.10:g.185488081G= NCBI36
NG_046950.1:g.321744G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302277.7:c.256-18494G= MANE Select ENSP00000303252.6:n.256-18494G=
ENST00000302277.6:c.256-18494G= ENSP00000303252.6:n.256-18494G=
ENST00000613975.1:c.1-18494G= ENSP00000483032.1:n.1-18494G=
NM_194250.1:c.256-18494G= NP_919226.1:n.256-18494G=
NM_194250.2:c.256-18494G= MANE Select NP_919226.1:n.256-18494G=
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