Canonical Allele Identifier: CA667283573

Gene: ZNF365

Linked Data

• dbSNP Id: rs1293565035
• gnomAD v3: 10-62631533-G-C
• gnomAD v4: 10-62631533-G-C
• MyVariant Identifiers: chr10:g.64391293G>C (hg19) ; chr10:g.62631533G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62631533G>C , CM000672.2:g.62631533G>C	GRCh38
NC_000010.10:g.64391293G>C , CM000672.1:g.64391293G>C	GRCh37
NC_000010.9:g.64061299G>C	NCBI36
NG_021209.1:g.262378G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647733.1:c.1129+8283G>C	ENSP00000502188.1:n.1129+8283G>C
ENST00000395251.5:c.-184-12209G>C	ENSP00000378672.1:n.-184-12209G>C
ENST00000410046.7:c.1129+8283G>C	ENSP00000387091.3:n.1129+8283G>C
NM_199451.2:c.1129+8283G>C	NP_955523.1:n.1129+8283G>C
NM_199452.3:c.-184-12209G>C	NP_955524.3:n.-184-12209G>C
XR_946002.1:n.82-6410C>G
XR_946002.2:n.82-6410C>G
NM_199451.3:c.1129+8283G>C	NP_955523.1:n.1129+8283G>C