Canonical Allele Identifier: CA1313491646
Gene: ZNF804A HGNC NCBI

Linked Data

dbSNP Id: rs1685437753
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.184915660C>A , CM000664.2:g.184915660C>A GRCh38
NC_000002.11:g.185780387C>A , CM000664.1:g.185780387C>A GRCh37
NC_000002.10:g.185488632C>A NCBI36
NG_046950.1:g.322295C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000302277.7:c.256-17943C>A MANE Select ENSP00000303252.6:n.256-17943C>A
ENST00000302277.6:c.256-17943C>A ENSP00000303252.6:n.256-17943C>A
ENST00000613975.1:c.1-17943C>A ENSP00000483032.1:n.1-17943C>A
NM_194250.1:c.256-17943C>A NP_919226.1:n.256-17943C>A
NM_194250.2:c.256-17943C>A MANE Select NP_919226.1:n.256-17943C>A
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