Canonical Allele Identifier: CA232593082
Gene: ZNF705A HGNC NCBI

Linked Data

dbSNP Id: rs1051849847
gnomAD v2: 12-8291247-A-T
gnomAD v3: 12-8138651-A-T
gnomAD v4: 12-8138651-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138651A>T , CM000674.2:g.8138651A>T GRCh38
NC_000012.11:g.8291247A>T , CM000674.1:g.8291247A>T GRCh37
NC_000012.10:g.8182514A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000402465.8:c.114+398A>T
ENST00000402465.7:c.-151+398A>T ENSP00000384896.3:n.-151+398A>T