Canonical Allele Identifier: CA667263031

Gene: ZNF365

Linked Data

• dbSNP Id: rs1247467917
• MyVariant Identifiers: chr10:g.64261156T>G (hg19) ; chr10:g.62501397T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62501397T>G , CM000672.2:g.62501397T>G	GRCh38
NC_000010.10:g.64261156T>G , CM000672.1:g.64261156T>G	GRCh37
NC_000010.9:g.63931162T>G	NCBI36
NG_021209.1:g.132241T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647733.1:c.981+41600T>G	ENSP00000502188.1:n.981+41600T>G
ENST00000410046.7:c.981+41600T>G	ENSP00000387091.3:n.981+41600T>G
NM_199451.2:c.981+41600T>G	NP_955523.1:n.981+41600T>G
XM_017015937.2:c.981+41600T>G	XP_016871426.1:n.981+41600T>G
NM_199451.3:c.981+41600T>G	NP_955523.1:n.981+41600T>G