Canonical Allele Identifier: CA13222168
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs7070565
gnomAD v2: 10-64278512-G-T
gnomAD v3: 10-62518753-G-T
gnomAD v4: 10-62518753-G-T
MyVariant Identifiers: chr10:g.64278512G>T (hg19) chr10:g.62518753G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62518753G>T , CM000672.2:g.62518753G>T GRCh38
NC_000010.10:g.64278512G>T , CM000672.1:g.64278512G>T GRCh37
NC_000010.9:g.63948518G>T NCBI36
NG_021209.1:g.149597G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+58956G>T ENSP00000502188.1:n.981+58956G>T
ENST00000410046.7:c.981+58956G>T ENSP00000387091.3:n.981+58956G>T
NM_199451.2:c.981+58956G>T NP_955523.1:n.981+58956G>T
XM_017015937.2:c.982-25456G>T XP_016871426.1:n.982-25456G>T
NM_199451.3:c.981+58956G>T NP_955523.1:n.981+58956G>T
Search 100 bp 5'
Search 100 bp 3'