Canonical Allele Identifier: CA15736314
Gene: ZNF705A HGNC NCBI
MyVariant.info:
GRCh38 chr12:g.8138610C>T
GRCh37 chr12:g.8291206C>T
gnomAD v2:
12:8291206 C / T
gnomAD v3:
12:8138610 C / T
gnomAD v4:
chr12-8138610-C-T
Joint Max Group AF 0.48059425 (EAS)
Genomes Max Group AF 0.48633939 (EAS)
Exomes Max Group AF 0.41157503 (EAS)
dbSNP:
10840759
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138610C>T , CM000674.2:g.8138610C>T GRCh38
NC_000012.11:g.8291206C>T , CM000674.1:g.8291206C>T GRCh37
NC_000012.10:g.8182473C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000402465.8:c.114+357C>T
ENST00000402465.7:c.-151+357C>T ENSP00000384896.3:n.-151+357C>T
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