Canonical Allele Identifier: CA667283578

Gene: ZNF365

Linked Data

• dbSNP Id: rs1310325671
• gnomAD v3: 10-62631556-C-G
• gnomAD v4: 10-62631556-C-G
• MyVariant Identifiers: chr10:g.64391316C>G (hg19) ; chr10:g.62631556C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62631556C>G , CM000672.2:g.62631556C>G	GRCh38
NC_000010.10:g.64391316C>G , CM000672.1:g.64391316C>G	GRCh37
NC_000010.9:g.64061322C>G	NCBI36
NG_021209.1:g.262401C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647733.1:c.1129+8306C>G	ENSP00000502188.1:n.1129+8306C>G
ENST00000395251.5:c.-184-12186C>G	ENSP00000378672.1:n.-184-12186C>G
ENST00000410046.7:c.1129+8306C>G	ENSP00000387091.3:n.1129+8306C>G
NM_199451.2:c.1129+8306C>G	NP_955523.1:n.1129+8306C>G
NM_199452.3:c.-184-12186C>G	NP_955524.3:n.-184-12186C>G
XR_946002.1:n.82-6433G>C
XR_946002.2:n.82-6433G>C
NM_199451.3:c.1129+8306C>G	NP_955523.1:n.1129+8306C>G