Canonical Allele Identifier: CA692441240
Gene: ZNF705A HGNC NCBI

Linked Data

dbSNP Id: rs1427749074
MyVariant Identifiers: chr12:g.8291257_8291258insAAA (hg19) chr12:g.8138661_8138662insAAA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138662_8138663insAAA , CM000674.2:g.8138662_8138663insAAA GRCh38
NC_000012.11:g.8291258_8291259insAAA , CM000674.1:g.8291258_8291259insAAA GRCh37
NC_000012.10:g.8182525_8182526insAAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000402465.8:c.114+409_114+410insAAA
ENST00000402465.7:c.-151+409_-151+410insAAA ENSP00000384896.3:n.-151+409_-151+410insAAA
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