Canonical Allele Identifier: CA11902229
Gene: ZNF732 HGNC NCBI
MyVariant.info:
GRCh38 chr4:g.288710A>G
GRCh37 chr4:g.282499A>G
gnomAD v2:
4:282499 A / G
gnomAD v3:
4:288710 A / G
gnomAD v4:
chr4-288710-A-G
Joint Max Group AF 0.2395737 (AMR)
Genomes Max Group AF 0.2395737 (AMR)
dbSNP:
11723261
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.288710A>G , CM000666.2:g.288710A>G GRCh38
NC_000004.11:g.282499A>G , CM000666.1:g.282499A>G GRCh37
NC_000004.10:g.272499A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000419098.6:c.226+6728T>C MANE Select ENSP00000415774.1:n.226+6728T>C
ENST00000419098.5:c.226+6728T>C ENSP00000415774.1:n.226+6728T>C
ENST00000619749.1:c.223+6728T>C ENSP00000478210.1:n.223+6728T>C
NM_001137608.1:c.226+6728T>C NP_001131080.1:n.226+6728T>C
NM_001137608.2:c.226+6728T>C NP_001131080.1:n.226+6728T>C
NM_001137608.3:c.226+6728T>C MANE Select NP_001131080.1:n.226+6728T>C
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