Canonical Allele Identifier: CA2563848795
Gene: ZNF705A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138664A>T , CM000674.2:g.8138664A>T GRCh38
NC_000012.11:g.8291260A>T , CM000674.1:g.8291260A>T GRCh37
NC_000012.10:g.8182527A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000402465.8:c.114+411A>T
ENST00000402465.7:c.-151+411A>T ENSP00000384896.3:n.-151+411A>T