Canonical Allele Identifier: CA603179477
Gene: ZNF705A HGNC NCBI

Linked Data

dbSNP Id: rs1398361608

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138610_8138612del , CM000674.2:g.8138610_8138612del GRCh38
NC_000012.11:g.8291206_8291208del , CM000674.1:g.8291206_8291208del GRCh37
NC_000012.10:g.8182473_8182475del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000402465.8:c.114+357_114+359del
ENST00000402465.7:c.-151+357_-151+359del ENSP00000384896.3:n.-151+357_-151+359del