Canonical Allele Identifier: CA667306041

Gene: ZNF365

Linked Data

• dbSNP Id: rs1332999459
• gnomAD v3: 10-62610226-A-G
• gnomAD v4: 10-62610226-A-G
• MyVariant Identifiers: chr10:g.64369985A>G (hg19) ; chr10:g.62610226A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62610226A>G , CM000672.2:g.62610226A>G	GRCh38
NC_000010.10:g.64369985A>G , CM000672.1:g.64369985A>G	GRCh37
NC_000010.9:g.64039991A>G	NCBI36
NG_021209.1:g.241070A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647733.1:c.982-12877A>G	ENSP00000502188.1:n.982-12877A>G
ENST00000395251.5:c.-184-33516A>G	ENSP00000378672.1:n.-184-33516A>G
ENST00000410046.7:c.982-12877A>G	ENSP00000387091.3:n.982-12877A>G
NM_199451.2:c.982-12877A>G	NP_955523.1:n.982-12877A>G
NM_199452.3:c.-184-33516A>G	NP_955524.3:n.-184-33516A>G
NM_199451.3:c.982-12877A>G	NP_955523.1:n.982-12877A>G