Canonical Allele Identifier: CA2725265330
Gene: ZNF705A HGNC NCBI

Linked Data

dbSNP Id: rs961148740

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138613G>C , CM000674.2:g.8138613G>C GRCh38
NC_000012.11:g.8291209G>C , CM000674.1:g.8291209G>C GRCh37
NC_000012.10:g.8182476G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000402465.8:c.114+360G>C
ENST00000402465.7:c.-151+360G>C ENSP00000384896.3:n.-151+360G>C