Canonical Allele Identifier: CA469907180

Gene: ZNF365

Linked Data

• dbSNP Id: rs1176978024
• gnomAD v3: 10-62620539-C-A
• gnomAD v4: 10-62620539-C-A
• MyVariant Identifiers: chr10:g.64380299C>A (hg19) ; chr10:g.62620539C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62620539C>A , CM000672.2:g.62620539C>A	GRCh38
NC_000010.10:g.64380299C>A , CM000672.1:g.64380299C>A	GRCh37
NC_000010.9:g.64050305C>A	NCBI36
NG_021209.1:g.251384C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647733.1:c.982-2564C>A	ENSP00000502188.1:n.982-2564C>A
ENST00000395251.5:c.-184-23203C>A	ENSP00000378672.1:n.-184-23203C>A
ENST00000410046.7:c.982-2564C>A	ENSP00000387091.3:n.982-2564C>A
NM_199451.2:c.982-2564C>A	NP_955523.1:n.982-2564C>A
NM_199452.3:c.-184-23203C>A	NP_955524.3:n.-184-23203C>A
NM_199451.3:c.982-2564C>A	NP_955523.1:n.982-2564C>A