Canonical Allele Identifier: CA692441241
Gene: ZNF705A HGNC NCBI

Linked Data

dbSNP Id: rs1195203708

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138665C>A , CM000674.2:g.8138665C>A GRCh38
NC_000012.11:g.8291261C>A , CM000674.1:g.8291261C>A GRCh37
NC_000012.10:g.8182528C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000402465.8:c.114+412C>A
ENST00000402465.7:c.-151+412C>A ENSP00000384896.3:n.-151+412C>A