Canonical Allele Identifier: CA13267750
Gene: ZNF365 HGNC NCBI
COSMIC:
COSN17141119 (not active)
COSN17143362 (not active)
COSN17144189 (not active)
MyVariant.info:
GRCh38 chr10:g.62518923G>A
GRCh37 chr10:g.64278682G>A
gnomAD v2:
10:64278682 G / A
gnomAD v3:
10:62518923 G / A
gnomAD v4:
chr10-62518923-G-A
Joint Max Group AF 0.17023795 (AFR)
Genomes Max Group AF 0.17023795 (AFR)
dbSNP:
10995190
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62518923G>A , CM000672.2:g.62518923G>A GRCh38
NC_000010.10:g.64278682G>A , CM000672.1:g.64278682G>A GRCh37
NC_000010.9:g.63948688G>A NCBI36
NG_021209.1:g.149767G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+59126G>A ENSP00000502188.1:n.981+59126G>A
ENST00000410046.7:c.981+59126G>A ENSP00000387091.3:n.981+59126G>A
NM_199451.2:c.981+59126G>A NP_955523.1:n.981+59126G>A
XM_017015937.2:c.982-25286G>A XP_016871426.1:n.982-25286G>A
NM_199451.3:c.981+59126G>A NP_955523.1:n.981+59126G>A
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