Canonical Allele Identifier: CA1432667948
Gene: ZNF732 HGNC NCBI

Linked Data

dbSNP Id: rs1560161396
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.288612A>T , CM000666.2:g.288612A>T GRCh38
NC_000004.11:g.282401A>T , CM000666.1:g.282401A>T GRCh37
NC_000004.10:g.272401A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000419098.6:c.226+6826T>A MANE Select ENSP00000415774.1:n.226+6826T>A
ENST00000419098.5:c.226+6826T>A ENSP00000415774.1:n.226+6826T>A
ENST00000619749.1:c.223+6826T>A ENSP00000478210.1:n.223+6826T>A
NM_001137608.1:c.226+6826T>A NP_001131080.1:n.226+6826T>A
NM_001137608.2:c.226+6826T>A NP_001131080.1:n.226+6826T>A
NM_001137608.3:c.226+6826T>A MANE Select NP_001131080.1:n.226+6826T>A
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