Canonical Allele Identifier: CA594047521
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1330762906
gnomAD v2: 10-64380196-C-A
gnomAD v3: 10-62620436-C-A
gnomAD v4: 10-62620436-C-A
MyVariant Identifiers: chr10:g.64380196C>A (hg19) chr10:g.62620436C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62620436C>A , CM000672.2:g.62620436C>A GRCh38
NC_000010.10:g.64380196C>A , CM000672.1:g.64380196C>A GRCh37
NC_000010.9:g.64050202C>A NCBI36
NG_021209.1:g.251281C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647733.1:c.982-2667C>A ENSP00000502188.1:n.982-2667C>A
ENST00000395251.5:c.-184-23306C>A ENSP00000378672.1:n.-184-23306C>A
ENST00000410046.7:c.982-2667C>A ENSP00000387091.3:n.982-2667C>A
NM_199451.2:c.982-2667C>A NP_955523.1:n.982-2667C>A
NM_199452.3:c.-184-23306C>A NP_955524.3:n.-184-23306C>A
NM_199451.3:c.982-2667C>A NP_955523.1:n.982-2667C>A
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