Canonical Allele Identifier: CA2617469269
Gene: ZNF705A HGNC NCBI

Linked Data

gnomAD v4: 12-8138622-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138622T>A , CM000674.2:g.8138622T>A GRCh38
NC_000012.11:g.8291218T>A , CM000674.1:g.8291218T>A GRCh37
NC_000012.10:g.8182485T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000402465.8:c.114+369T>A
ENST00000402465.7:c.-151+369T>A ENSP00000384896.3:n.-151+369T>A