Canonical Allele Identifier: CA692441253
Gene: ZNF705A HGNC NCBI

Linked Data

dbSNP Id: rs1262354780
MyVariant Identifiers: chr12:g.8291262_8291263insGC (hg19) chr12:g.8138666_8138667insGC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138667_8138668insCG , CM000674.2:g.8138667_8138668insCG GRCh38
NC_000012.11:g.8291263_8291264insCG , CM000674.1:g.8291263_8291264insCG GRCh37
NC_000012.10:g.8182530_8182531insCG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000402465.8:c.114+414_114+415insCG
ENST00000402465.7:c.-151+414_-151+415insCG ENSP00000384896.3:n.-151+414_-151+415insCG
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