Canonical Allele Identifier: CA15633102
Gene: ZNF365 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10822013

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62492218C>T , CM000672.2:g.62492218C>T GRCh38
NC_000010.10:g.64251977C>T , CM000672.1:g.64251977C>T GRCh37
NC_000010.9:g.63921983C>T NCBI36
NG_021209.1:g.123062C>T

Transcript Alleles

HGVS Amino-acid change
NM_199451.2:c.981+32421C>T VV NP_955523.1:p.=
XM_017015937.2:c.981+32421C>T XP_016871426.1:p.=
ENST00000410046.7:c.981+32421C>T ENSP00000387091.3:p.=