Canonical Allele Identifier: CA91014682
Gene: ZNF732 HGNC NCBI

Linked Data

dbSNP Id: rs969490777
gnomAD v2: 4-282416-T-G
gnomAD v3: 4-288627-T-G
gnomAD v4: 4-288627-T-G
MyVariant Identifiers: chr4:g.282416T>G (hg19) chr4:g.288627T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.288627T>G , CM000666.2:g.288627T>G GRCh38
NC_000004.11:g.282416T>G , CM000666.1:g.282416T>G GRCh37
NC_000004.10:g.272416T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000419098.6:c.226+6811A>C MANE Select ENSP00000415774.1:n.226+6811A>C
ENST00000419098.5:c.226+6811A>C ENSP00000415774.1:n.226+6811A>C
ENST00000619749.1:c.223+6811A>C ENSP00000478210.1:n.223+6811A>C
NM_001137608.1:c.226+6811A>C NP_001131080.1:n.226+6811A>C
NM_001137608.2:c.226+6811A>C NP_001131080.1:n.226+6811A>C
NM_001137608.3:c.226+6811A>C MANE Select NP_001131080.1:n.226+6811A>C
Search 100 bp 5'
Search 100 bp 3'