Canonical Allele Identifier: CA208589091
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs957974732
gnomAD v3: 10-62501476-A-C
gnomAD v4: 10-62501476-A-C
MyVariant Identifiers: chr10:g.64261235A>C (hg19) chr10:g.62501476A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62501476A>C , CM000672.2:g.62501476A>C GRCh38
NC_000010.10:g.64261235A>C , CM000672.1:g.64261235A>C GRCh37
NC_000010.9:g.63931241A>C NCBI36
NG_021209.1:g.132320A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647733.1:c.981+41679A>C ENSP00000502188.1:n.981+41679A>C
ENST00000410046.7:c.981+41679A>C ENSP00000387091.3:n.981+41679A>C
NM_199451.2:c.981+41679A>C NP_955523.1:n.981+41679A>C
XM_017015937.2:c.981+41679A>C XP_016871426.1:n.981+41679A>C
NM_199451.3:c.981+41679A>C NP_955523.1:n.981+41679A>C
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