Canonical Allele Identifier: CA761931777

Gene: ZNF804A

Linked Data

• dbSNP Id: rs1378729358
• MyVariant Identifiers: chr2:g.185780212C>T (hg19) ; chr2:g.184915485C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.184915485C>T , CM000664.2:g.184915485C>T	GRCh38
NC_000002.11:g.185780212C>T , CM000664.1:g.185780212C>T	GRCh37
NC_000002.10:g.185488457C>T	NCBI36
NG_046950.1:g.322120C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302277.7:c.256-18118C>T MANE Select	ENSP00000303252.6:n.256-18118C>T
ENST00000302277.6:c.256-18118C>T	ENSP00000303252.6:n.256-18118C>T
ENST00000613975.1:c.1-18118C>T	ENSP00000483032.1:n.1-18118C>T
NM_194250.1:c.256-18118C>T	NP_919226.1:n.256-18118C>T
NM_194250.2:c.256-18118C>T MANE Select	NP_919226.1:n.256-18118C>T