Canonical Allele Identifier: CA2014883846
Gene: ZNF705A HGNC NCBI

Linked Data

dbSNP Id: rs1948169853
gnomAD v4: 12-8138618-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138618G>T , CM000674.2:g.8138618G>T GRCh38
NC_000012.11:g.8291214G>T , CM000674.1:g.8291214G>T GRCh37
NC_000012.10:g.8182481G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000402465.8:c.114+365G>T
ENST00000402465.7:c.-151+365G>T ENSP00000384896.3:n.-151+365G>T