Canonical Allele Identifier: CA594033339

Gene: ZNF365

Linked Data

• dbSNP Id: rs1309155432
• gnomAD v2: 10-64278485-G-A
• gnomAD v3: 10-62518726-G-A
• gnomAD v4: 10-62518726-G-A
• MyVariant Identifiers: chr10:g.64278485G>A (hg19) ; chr10:g.62518726G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62518726G>A , CM000672.2:g.62518726G>A	GRCh38
NC_000010.10:g.64278485G>A , CM000672.1:g.64278485G>A	GRCh37
NC_000010.9:g.63948491G>A	NCBI36
NG_021209.1:g.149570G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647733.1:c.981+58929G>A	ENSP00000502188.1:n.981+58929G>A
ENST00000410046.7:c.981+58929G>A	ENSP00000387091.3:n.981+58929G>A
NM_199451.2:c.981+58929G>A	NP_955523.1:n.981+58929G>A
XM_017015937.2:c.982-25483G>A	XP_016871426.1:n.982-25483G>A
NM_199451.3:c.981+58929G>A	NP_955523.1:n.981+58929G>A