Canonical Allele Identifier: CA2014883852
Gene: ZNF705A HGNC NCBI

Linked Data

dbSNP Id: rs1948170158
gnomAD v4: 12-8138642-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138642T>G , CM000674.2:g.8138642T>G GRCh38
NC_000012.11:g.8291238T>G , CM000674.1:g.8291238T>G GRCh37
NC_000012.10:g.8182505T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000402465.8:c.114+389T>G
ENST00000402465.7:c.-151+389T>G ENSP00000384896.3:n.-151+389T>G