Canonical Allele Identifier: CA667256760
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1310019193
MyVariant Identifiers: chr10:g.64251798A>G (hg19) chr10:g.62492039A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62492039A>G , CM000672.2:g.62492039A>G GRCh38
NC_000010.10:g.64251798A>G , CM000672.1:g.64251798A>G GRCh37
NC_000010.9:g.63921804A>G NCBI36
NG_021209.1:g.122883A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+32242A>G ENSP00000502188.1:n.981+32242A>G
ENST00000410046.7:c.981+32242A>G ENSP00000387091.3:n.981+32242A>G
NM_199451.2:c.981+32242A>G NP_955523.1:n.981+32242A>G
XM_017015937.2:c.981+32242A>G XP_016871426.1:n.981+32242A>G
NM_199451.3:c.981+32242A>G NP_955523.1:n.981+32242A>G
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