Canonical Allele Identifier: CA944514513
Gene: ZNF705A HGNC NCBI

Linked Data

dbSNP Id: rs1948170492

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138663_8138664dup , CM000674.2:g.8138663_8138664dup GRCh38
NC_000012.11:g.8291259_8291260dup , CM000674.1:g.8291259_8291260dup GRCh37
NC_000012.10:g.8182526_8182527dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000402465.8:c.114+410_114+411dup
ENST00000402465.7:c.-151+410_-151+411dup ENSP00000384896.3:n.-151+410_-151+411dup