Canonical Allele Identifier: CA2617469282
Gene: ZNF705A HGNC NCBI

Linked Data

gnomAD v4: 12-8138633-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138633C>T , CM000674.2:g.8138633C>T GRCh38
NC_000012.11:g.8291229C>T , CM000674.1:g.8291229C>T GRCh37
NC_000012.10:g.8182496C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000402465.8:c.114+380C>T
ENST00000402465.7:c.-151+380C>T ENSP00000384896.3:n.-151+380C>T