Canonical Allele Identifier: CA232593079
Gene: ZNF705A HGNC NCBI

Linked Data

dbSNP Id: rs955283236
gnomAD v2: 12-8291244-A-G
gnomAD v3: 12-8138648-A-G
gnomAD v4: 12-8138648-A-G
MyVariant Identifiers: chr12:g.8291244A>G (hg19) chr12:g.8138648A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138648A>G , CM000674.2:g.8138648A>G GRCh38
NC_000012.11:g.8291244A>G , CM000674.1:g.8291244A>G GRCh37
NC_000012.10:g.8182511A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000402465.8:c.114+395A>G
ENST00000402465.7:c.-151+395A>G ENSP00000384896.3:n.-151+395A>G
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