Canonical Allele Identifier: CA12474899

Gene: ZNF804B

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.89065756A>T , CM000669.2:g.89065756A>T	GRCh38
NC_000007.13:g.88695070A>T , CM000669.1:g.88695070A>T	GRCh37
NC_000007.12:g.88533006A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333190.5:c.109-152399A>T MANE Select	ENSP00000329638.4:n.109-152399A>T
ENST00000333190.4:c.109-152399A>T	ENSP00000329638.4:n.109-152399A>T
NM_181646.3:c.109-152399A>T	NP_857597.1:n.109-152399A>T
NM_181646.4:c.109-152399A>T	NP_857597.1:n.109-152399A>T
NM_181646.5:c.109-152399A>T MANE Select	NP_857597.1:n.109-152399A>T