Canonical Allele Identifier: CA594033344
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1348381724
gnomAD v2: 10-64278618-ACAGT-A
gnomAD v3: 10-62518859-ACAGT-A
gnomAD v4: 10-62518859-ACAGT-A
MyVariant Identifiers: chr10:g.64278619_64278622del (hg19) chr10:g.62518860_62518863del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62518863_62518866del , CM000672.2:g.62518863_62518866del GRCh38
NC_000010.10:g.64278622_64278625del , CM000672.1:g.64278622_64278625del GRCh37
NC_000010.9:g.63948628_63948631del NCBI36
NG_021209.1:g.149707_149710del

Transcript Alleles

HGVS Amino-acid change
ENST00000647733.1:c.981+59066_981+59069del ENSP00000502188.1:n.981+59066_981+59069de...
ENST00000410046.7:c.981+59066_981+59069del ENSP00000387091.3:n.981+59066_981+59069de...
NM_199451.2:c.981+59066_981+59069del NP_955523.1:n.981+59066_981+59069del
XM_017015937.2:c.982-25346_982-25343del XP_016871426.1:n.982-25346_982-25343del
NM_199451.3:c.981+59066_981+59069del NP_955523.1:n.981+59066_981+59069del
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