Canonical Allele Identifier: CA1432667980
Gene: ZNF732 HGNC NCBI

Linked Data

dbSNP Id: rs1581540650
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.288672G>A , CM000666.2:g.288672G>A GRCh38
NC_000004.11:g.282461G>A , CM000666.1:g.282461G>A GRCh37
NC_000004.10:g.272461G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000419098.6:c.226+6766C>T MANE Select ENSP00000415774.1:n.226+6766C>T
ENST00000419098.5:c.226+6766C>T ENSP00000415774.1:n.226+6766C>T
ENST00000619749.1:c.223+6766C>T ENSP00000478210.1:n.223+6766C>T
NM_001137608.1:c.226+6766C>T NP_001131080.1:n.226+6766C>T
NM_001137608.2:c.226+6766C>T NP_001131080.1:n.226+6766C>T
NM_001137608.3:c.226+6766C>T MANE Select NP_001131080.1:n.226+6766C>T
Search 100 bp 5'
Search 100 bp 3'