Canonical Allele Identifier: CA667275111

Gene: ZNF365

Linked Data

• dbSNP Id: rs1214489523
• gnomAD v3: 10-62528654-G-T
• gnomAD v4: 10-62528654-G-T
• MyVariant Identifiers: chr10:g.64288413G>T (hg19) ; chr10:g.62528654G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62528654G>T , CM000672.2:g.62528654G>T	GRCh38
NC_000010.10:g.64288413G>T , CM000672.1:g.64288413G>T	GRCh37
NC_000010.9:g.63958419G>T	NCBI36
NG_021209.1:g.159498G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647733.1:c.981+68857G>T	ENSP00000502188.1:n.981+68857G>T
ENST00000395251.5:c.-185+8057G>T	ENSP00000378672.1:n.-185+8057G>T
ENST00000410046.7:c.981+68857G>T	ENSP00000387091.3:n.981+68857G>T
NM_199451.2:c.981+68857G>T	NP_955523.1:n.981+68857G>T
NM_199452.3:c.-185+8057G>T	NP_955524.3:n.-185+8057G>T
XM_017015937.2:c.982-15555G>T	XP_016871426.1:n.982-15555G>T
NM_199451.3:c.981+68857G>T	NP_955523.1:n.981+68857G>T