Canonical Allele Identifier: CA667283570

Gene: ZNF365

Linked Data

• dbSNP Id: rs1203865146
• gnomAD v3: 10-62631515-G-A
• gnomAD v4: 10-62631515-G-A
• MyVariant Identifiers: chr10:g.64391275G>A (hg19) ; chr10:g.62631515G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62631515G>A , CM000672.2:g.62631515G>A	GRCh38
NC_000010.10:g.64391275G>A , CM000672.1:g.64391275G>A	GRCh37
NC_000010.9:g.64061281G>A	NCBI36
NG_021209.1:g.262360G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000647733.1:c.1129+8265G>A	ENSP00000502188.1:n.1129+8265G>A
ENST00000395251.5:c.-184-12227G>A	ENSP00000378672.1:n.-184-12227G>A
ENST00000410046.7:c.1129+8265G>A	ENSP00000387091.3:n.1129+8265G>A
NM_199451.2:c.1129+8265G>A	NP_955523.1:n.1129+8265G>A
NM_199452.3:c.-184-12227G>A	NP_955524.3:n.-184-12227G>A
XR_946002.1:n.82-6392C>T
XR_946002.2:n.82-6392C>T
NM_199451.3:c.1129+8265G>A	NP_955523.1:n.1129+8265G>A