Canonical Allele Identifier: CA62394069
Gene: ZNF804A HGNC NCBI

Linked Data

dbSNP Id: rs1018502504
MyVariant Identifiers: chr2:g.185778665T>C (hg19) chr2:g.184913938T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.184913938T>C , CM000664.2:g.184913938T>C GRCh38
NC_000002.11:g.185778665T>C , CM000664.1:g.185778665T>C GRCh37
NC_000002.10:g.185486910T>C NCBI36
NG_046950.1:g.320573T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000302277.7:c.256-19665T>C MANE Select ENSP00000303252.6:n.256-19665T>C
ENST00000302277.6:c.256-19665T>C ENSP00000303252.6:n.256-19665T>C
ENST00000613975.1:c.1-19665T>C ENSP00000483032.1:n.1-19665T>C
NM_194250.1:c.256-19665T>C NP_919226.1:n.256-19665T>C
NM_194250.2:c.256-19665T>C MANE Select NP_919226.1:n.256-19665T>C
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