Canonical Allele Identifier: CA692441234
Gene: ZNF705A HGNC NCBI

Linked Data

dbSNP Id: rs1401929083

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138649T>C , CM000674.2:g.8138649T>C GRCh38
NC_000012.11:g.8291245T>C , CM000674.1:g.8291245T>C GRCh37
NC_000012.10:g.8182512T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000402465.8:c.114+396T>C
ENST00000402465.7:c.-151+396T>C ENSP00000384896.3:n.-151+396T>C