Canonical Allele Identifier: CA761931653
Gene: ZNF804A HGNC NCBI

Linked Data

dbSNP Id: rs1304250264
MyVariant Identifiers: chr2:g.185779837T>A (hg19) chr2:g.184915110T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.184915110T>A , CM000664.2:g.184915110T>A GRCh38
NC_000002.11:g.185779837T>A , CM000664.1:g.185779837T>A GRCh37
NC_000002.10:g.185488082T>A NCBI36
NG_046950.1:g.321745T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000302277.7:c.256-18493T>A MANE Select ENSP00000303252.6:n.256-18493T>A
ENST00000302277.6:c.256-18493T>A ENSP00000303252.6:n.256-18493T>A
ENST00000613975.1:c.1-18493T>A ENSP00000483032.1:n.1-18493T>A
NM_194250.1:c.256-18493T>A NP_919226.1:n.256-18493T>A
NM_194250.2:c.256-18493T>A MANE Select NP_919226.1:n.256-18493T>A
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