Canonical Allele Identifier: CA944514502
Gene: ZNF705A HGNC NCBI

Linked Data

dbSNP Id: rs1948169990
gnomAD v3: 12-8138631-C-A
gnomAD v4: 12-8138631-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138631C>A , CM000674.2:g.8138631C>A GRCh38
NC_000012.11:g.8291227C>A , CM000674.1:g.8291227C>A GRCh37
NC_000012.10:g.8182494C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000402465.8:c.114+378C>A
ENST00000402465.7:c.-151+378C>A ENSP00000384896.3:n.-151+378C>A
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