Canonical Allele Identifier: CA62394055
Gene: ZNF804A HGNC NCBI

Linked Data

dbSNP Id: rs1038052770
MyVariant Identifiers: chr2:g.185778433T>C (hg19) chr2:g.184913706T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.184913706T>C , CM000664.2:g.184913706T>C GRCh38
NC_000002.11:g.185778433T>C , CM000664.1:g.185778433T>C GRCh37
NC_000002.10:g.185486678T>C NCBI36
NG_046950.1:g.320341T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000302277.7:c.256-19897T>C MANE Select ENSP00000303252.6:n.256-19897T>C
ENST00000302277.6:c.256-19897T>C ENSP00000303252.6:n.256-19897T>C
ENST00000613975.1:c.1-19897T>C ENSP00000483032.1:n.1-19897T>C
NM_194250.1:c.256-19897T>C NP_919226.1:n.256-19897T>C
NM_194250.2:c.256-19897T>C MANE Select NP_919226.1:n.256-19897T>C
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