Canonical Allele Identifier: CA208587974
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs979751201
gnomAD v3: 10-62491971-C-T
gnomAD v4: 10-62491971-C-T
MyVariant Identifiers: chr10:g.64251730C>T (hg19) chr10:g.62491971C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62491971C>T , CM000672.2:g.62491971C>T GRCh38
NC_000010.10:g.64251730C>T , CM000672.1:g.64251730C>T GRCh37
NC_000010.9:g.63921736C>T NCBI36
NG_021209.1:g.122815C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+32174C>T ENSP00000502188.1:n.981+32174C>T
ENST00000410046.7:c.981+32174C>T ENSP00000387091.3:n.981+32174C>T
NM_199451.2:c.981+32174C>T NP_955523.1:n.981+32174C>T
XM_017015937.2:c.981+32174C>T XP_016871426.1:n.981+32174C>T
NM_199451.3:c.981+32174C>T NP_955523.1:n.981+32174C>T
Search 100 bp 5'
Search 100 bp 3'