Canonical Allele Identifier: CA1313504337
Gene: ZNF804A HGNC NCBI

Linked Data

dbSNP Id: rs1685438274
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.184915708G>T , CM000664.2:g.184915708G>T GRCh38
NC_000002.11:g.185780435G>T , CM000664.1:g.185780435G>T GRCh37
NC_000002.10:g.185488680G>T NCBI36
NG_046950.1:g.322343G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000302277.7:c.256-17895G>T MANE Select ENSP00000303252.6:n.256-17895G>T
ENST00000302277.6:c.256-17895G>T ENSP00000303252.6:n.256-17895G>T
ENST00000613975.1:c.1-17895G>T ENSP00000483032.1:n.1-17895G>T
NM_194250.1:c.256-17895G>T NP_919226.1:n.256-17895G>T
NM_194250.2:c.256-17895G>T MANE Select NP_919226.1:n.256-17895G>T
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