Canonical Allele Identifier: CA208587992
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs114573250
gnomAD v2: 10-64251918-C-T
gnomAD v3: 10-62492159-C-T
gnomAD v4: 10-62492159-C-T
MyVariant Identifiers: chr10:g.64251918C>T (hg19) chr10:g.62492159C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62492159C>T , CM000672.2:g.62492159C>T GRCh38
NC_000010.10:g.64251918C>T , CM000672.1:g.64251918C>T GRCh37
NC_000010.9:g.63921924C>T NCBI36
NG_021209.1:g.123003C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+32362C>T ENSP00000502188.1:n.981+32362C>T
ENST00000410046.7:c.981+32362C>T ENSP00000387091.3:n.981+32362C>T
NM_199451.2:c.981+32362C>T NP_955523.1:n.981+32362C>T
XM_017015937.2:c.981+32362C>T XP_016871426.1:n.981+32362C>T
NM_199451.3:c.981+32362C>T NP_955523.1:n.981+32362C>T
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