Canonical Allele Identifier: CA208592500

Gene: ZNF365

Linked Data

• dbSNP Id: rs376262322
• MyVariant Identifiers: chr10:g.64291085G>T (hg19) ; chr10:g.62531326G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62531326G>T , CM000672.2:g.62531326G>T	GRCh38
NC_000010.10:g.64291085G>T , CM000672.1:g.64291085G>T	GRCh37
NC_000010.9:g.63961091G>T	NCBI36
NG_021209.1:g.162170G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647733.1:c.981+71529G>T	ENSP00000502188.1:n.981+71529G>T
ENST00000395251.5:c.-185+10729G>T	ENSP00000378672.1:n.-185+10729G>T
ENST00000410046.7:c.981+71529G>T	ENSP00000387091.3:n.981+71529G>T
NM_199451.2:c.981+71529G>T	NP_955523.1:n.981+71529G>T
NM_199452.3:c.-185+10729G>T	NP_955524.3:n.-185+10729G>T
XM_017015937.2:c.982-12883G>T	XP_016871426.1:n.982-12883G>T
NM_199451.3:c.981+71529G>T	NP_955523.1:n.981+71529G>T