Canonical Allele Identifier: CA594042529

Gene: ZNF365

Linked Data

• dbSNP Id: rs1487270008
• gnomAD v2: 10-64251938-C-T
• gnomAD v3: 10-62492179-C-T
• gnomAD v4: 10-62492179-C-T
• MyVariant Identifiers: chr10:g.64251938C>T (hg19) ; chr10:g.62492179C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62492179C>T , CM000672.2:g.62492179C>T	GRCh38
NC_000010.10:g.64251938C>T , CM000672.1:g.64251938C>T	GRCh37
NC_000010.9:g.63921944C>T	NCBI36
NG_021209.1:g.123023C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647733.1:c.981+32382C>T	ENSP00000502188.1:n.981+32382C>T
ENST00000410046.7:c.981+32382C>T	ENSP00000387091.3:n.981+32382C>T
NM_199451.2:c.981+32382C>T	NP_955523.1:n.981+32382C>T
XM_017015937.2:c.981+32382C>T	XP_016871426.1:n.981+32382C>T
NM_199451.3:c.981+32382C>T	NP_955523.1:n.981+32382C>T