Canonical Allele Identifier: CA2617469273
Gene: ZNF705A HGNC NCBI

Linked Data

gnomAD v4: 12-8138626-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138626T>C , CM000674.2:g.8138626T>C GRCh38
NC_000012.11:g.8291222T>C , CM000674.1:g.8291222T>C GRCh37
NC_000012.10:g.8182489T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000402465.8:c.114+373T>C
ENST00000402465.7:c.-151+373T>C ENSP00000384896.3:n.-151+373T>C