Canonical Allele Identifier: CA232593090
Gene: ZNF705A HGNC NCBI

Linked Data

dbSNP Id: rs200489842
MyVariant Identifiers: chr12:g.8291259T>A (hg19) chr12:g.8138663T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138663T>A , CM000674.2:g.8138663T>A GRCh38
NC_000012.11:g.8291259T>A , CM000674.1:g.8291259T>A GRCh37
NC_000012.10:g.8182526T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000402465.8:c.114+410T>A
ENST00000402465.7:c.-151+410T>A ENSP00000384896.3:n.-151+410T>A
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