Canonical Allele Identifier: CA232593085
Gene: ZNF705A HGNC NCBI

Linked Data

dbSNP Id: rs371727333
gnomAD v2: 12-8291249-T-A
gnomAD v3: 12-8138653-T-A
gnomAD v4: 12-8138653-T-A
MyVariant Identifiers: chr12:g.8291249T>A (hg19) chr12:g.8138653T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138653T>A , CM000674.2:g.8138653T>A GRCh38
NC_000012.11:g.8291249T>A , CM000674.1:g.8291249T>A GRCh37
NC_000012.10:g.8182516T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000402465.8:c.114+400T>A
ENST00000402465.7:c.-151+400T>A ENSP00000384896.3:n.-151+400T>A
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