Canonical Allele Identifier: CA1432667906

Gene: ZNF732

Linked Data

• dbSNP Id: rs1719777700

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.288523A>G , CM000666.2:g.288523A>G	GRCh38
NC_000004.11:g.282312A>G , CM000666.1:g.282312A>G	GRCh37
NC_000004.10:g.272312A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419098.6:c.226+6915T>C MANE Select	ENSP00000415774.1:n.226+6915T>C
ENST00000419098.5:c.226+6915T>C	ENSP00000415774.1:n.226+6915T>C
ENST00000619749.1:c.223+6915T>C	ENSP00000478210.1:n.223+6915T>C
NM_001137608.1:c.226+6915T>C	NP_001131080.1:n.226+6915T>C
NM_001137608.2:c.226+6915T>C	NP_001131080.1:n.226+6915T>C
NM_001137608.3:c.226+6915T>C MANE Select	NP_001131080.1:n.226+6915T>C