Canonical Allele Identifier: CA793574714

Gene: ZNF732

Linked Data

• dbSNP Id: rs144580614
• gnomAD v3: 4-288661-C-T
• gnomAD v4: 4-288661-C-T
• MyVariant Identifiers: chr4:g.282450C>T (hg19) ; chr4:g.288661C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.288661C>T , CM000666.2:g.288661C>T	GRCh38
NC_000004.11:g.282450C>T , CM000666.1:g.282450C>T	GRCh37
NC_000004.10:g.272450C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000419098.6:c.226+6777G>A MANE Select	ENSP00000415774.1:n.226+6777G>A
ENST00000419098.5:c.226+6777G>A	ENSP00000415774.1:n.226+6777G>A
ENST00000619749.1:c.223+6777G>A	ENSP00000478210.1:n.223+6777G>A
NM_001137608.1:c.226+6777G>A	NP_001131080.1:n.226+6777G>A
NM_001137608.2:c.226+6777G>A	NP_001131080.1:n.226+6777G>A
NM_001137608.3:c.226+6777G>A MANE Select	NP_001131080.1:n.226+6777G>A