Canonical Allele Identifier: CA208587979

Gene: ZNF365

Linked Data

• dbSNP Id: rs575682091
• gnomAD v3: 10-62492056-T-G
• gnomAD v4: 10-62492056-T-G
• MyVariant Identifiers: chr10:g.64251815T>G (hg19) ; chr10:g.62492056T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62492056T>G , CM000672.2:g.62492056T>G	GRCh38
NC_000010.10:g.64251815T>G , CM000672.1:g.64251815T>G	GRCh37
NC_000010.9:g.63921821T>G	NCBI36
NG_021209.1:g.122900T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647733.1:c.981+32259T>G	ENSP00000502188.1:n.981+32259T>G
ENST00000410046.7:c.981+32259T>G	ENSP00000387091.3:n.981+32259T>G
NM_199451.2:c.981+32259T>G	NP_955523.1:n.981+32259T>G
XM_017015937.2:c.981+32259T>G	XP_016871426.1:n.981+32259T>G
NM_199451.3:c.981+32259T>G	NP_955523.1:n.981+32259T>G