Canonical Allele Identifier: CA761931643
Gene: ZNF804A HGNC NCBI

Linked Data

dbSNP Id: rs1307717145
gnomAD v3: 2-184915075-AT-A
gnomAD v4: 2-184915075-AT-A
MyVariant Identifiers: chr2:g.185779803del (hg19) chr2:g.184915076del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.184915078del , CM000664.2:g.184915078del GRCh38
NC_000002.11:g.185779805del , CM000664.1:g.185779805del GRCh37
NC_000002.10:g.185488050del NCBI36
NG_046950.1:g.321713del

Transcript Alleles

HGVS Amino-acid Change
ENST00000302277.7:c.256-18525del MANE Select ENSP00000303252.6:n.256-18525del
ENST00000302277.6:c.256-18525del ENSP00000303252.6:n.256-18525del
ENST00000613975.1:c.1-18525del ENSP00000483032.1:n.1-18525del
NM_194250.1:c.256-18525del NP_919226.1:n.256-18525del
NM_194250.2:c.256-18525del MANE Select NP_919226.1:n.256-18525del
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