Canonical Allele Identifier: CA208591101

Gene: ZNF365

Linked Data

• dbSNP Id: rs919736972
• gnomAD v3: 10-62519032-T-C
• gnomAD v4: 10-62519032-T-C
• MyVariant Identifiers: chr10:g.64278791T>C (hg19) ; chr10:g.62519032T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62519032T>C , CM000672.2:g.62519032T>C	GRCh38
NC_000010.10:g.64278791T>C , CM000672.1:g.64278791T>C	GRCh37
NC_000010.9:g.63948797T>C	NCBI36
NG_021209.1:g.149876T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647733.1:c.981+59235T>C	ENSP00000502188.1:n.981+59235T>C
ENST00000410046.7:c.981+59235T>C	ENSP00000387091.3:n.981+59235T>C
NM_199451.2:c.981+59235T>C	NP_955523.1:n.981+59235T>C
XM_017015937.2:c.982-25177T>C	XP_016871426.1:n.982-25177T>C
NM_199451.3:c.981+59235T>C	NP_955523.1:n.981+59235T>C