Canonical Allele Identifier: CA208587973
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1023199219
MyVariant Identifiers: chr10:g.64251716G>T (hg19) chr10:g.62491957G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62491957G>T , CM000672.2:g.62491957G>T GRCh38
NC_000010.10:g.64251716G>T , CM000672.1:g.64251716G>T GRCh37
NC_000010.9:g.63921722G>T NCBI36
NG_021209.1:g.122801G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+32160G>T ENSP00000502188.1:n.981+32160G>T
ENST00000410046.7:c.981+32160G>T ENSP00000387091.3:n.981+32160G>T
NM_199451.2:c.981+32160G>T NP_955523.1:n.981+32160G>T
XM_017015937.2:c.981+32160G>T XP_016871426.1:n.981+32160G>T
NM_199451.3:c.981+32160G>T NP_955523.1:n.981+32160G>T
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