Canonical Allele Identifier: CA232593069
Gene: ZNF705A HGNC NCBI

Linked Data

dbSNP Id: rs961148740
gnomAD v3: 12-8138613-G-A
gnomAD v4: 12-8138613-G-A
MyVariant Identifiers: chr12:g.8291209G>A (hg19) chr12:g.8138613G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138613G>A , CM000674.2:g.8138613G>A GRCh38
NC_000012.11:g.8291209G>A , CM000674.1:g.8291209G>A GRCh37
NC_000012.10:g.8182476G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000402465.8:c.114+360G>A
ENST00000402465.7:c.-151+360G>A ENSP00000384896.3:n.-151+360G>A
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