Canonical Allele Identifier: CA594033346

Gene: ZNF365

Linked Data

• dbSNP Id: rs745884076
• gnomAD v2: 10-64278619-C-G
• gnomAD v3: 10-62518860-C-G
• gnomAD v4: 10-62518860-C-G
• MyVariant Identifiers: chr10:g.64278619C>G (hg19) ; chr10:g.62518860C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62518860C>G , CM000672.2:g.62518860C>G	GRCh38
NC_000010.10:g.64278619C>G , CM000672.1:g.64278619C>G	GRCh37
NC_000010.9:g.63948625C>G	NCBI36
NG_021209.1:g.149704C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647733.1:c.981+59063C>G	ENSP00000502188.1:n.981+59063C>G
ENST00000410046.7:c.981+59063C>G	ENSP00000387091.3:n.981+59063C>G
NM_199451.2:c.981+59063C>G	NP_955523.1:n.981+59063C>G
XM_017015937.2:c.982-25349C>G	XP_016871426.1:n.982-25349C>G
NM_199451.3:c.981+59063C>G	NP_955523.1:n.981+59063C>G