Canonical Allele Identifier: CA793574716
Gene: ZNF732 HGNC NCBI

Linked Data

dbSNP Id: rs1360684599
gnomAD v3: 4-288675-C-A
gnomAD v4: 4-288675-C-A
MyVariant Identifiers: chr4:g.288675C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.288675C>A , CM000666.2:g.288675C>A GRCh38
NC_000004.11:g.282464C>A , CM000666.1:g.282464C>A GRCh37
NC_000004.10:g.272464C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000419098.6:c.226+6763G>T MANE Select ENSP00000415774.1:n.226+6763G>T
ENST00000419098.5:c.226+6763G>T ENSP00000415774.1:n.226+6763G>T
ENST00000619749.1:c.223+6763G>T ENSP00000478210.1:n.223+6763G>T
NM_001137608.1:c.226+6763G>T NP_001131080.1:n.226+6763G>T
NM_001137608.2:c.226+6763G>T NP_001131080.1:n.226+6763G>T
NM_001137608.3:c.226+6763G>T MANE Select NP_001131080.1:n.226+6763G>T
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