Canonical Allele Identifier: CA208592551

Gene: ZNF365

Linked Data

• dbSNP Id: rs560096395
• gnomAD v3: 10-62531652-A-G
• gnomAD v4: 10-62531652-A-G
• MyVariant Identifiers: chr10:g.64291411A>G (hg19) ; chr10:g.62531652A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62531652A>G , CM000672.2:g.62531652A>G	GRCh38
NC_000010.10:g.64291411A>G , CM000672.1:g.64291411A>G	GRCh37
NC_000010.9:g.63961417A>G	NCBI36
NG_021209.1:g.162496A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647733.1:c.981+71855A>G	ENSP00000502188.1:n.981+71855A>G
ENST00000395251.5:c.-185+11055A>G	ENSP00000378672.1:n.-185+11055A>G
ENST00000410046.7:c.981+71855A>G	ENSP00000387091.3:n.981+71855A>G
NM_199451.2:c.981+71855A>G	NP_955523.1:n.981+71855A>G
NM_199452.3:c.-185+11055A>G	NP_955524.3:n.-185+11055A>G
XM_017015937.2:c.982-12557A>G	XP_016871426.1:n.982-12557A>G
NM_199451.3:c.981+71855A>G	NP_955523.1:n.981+71855A>G