Canonical Allele Identifier: CA286385934

Gene: ZNF469

Linked Data

• ClinVar Variation Id: 1537488
• ClinVar RCV Id: RCV002159363 ; RCV002386956
• dbSNP Id: rs1008527622
• gnomAD v2: 16-88503796-G-A
• gnomAD v3: 16-88437388-G-A
• gnomAD v4: 16-88437388-G-A
• MyVariant Identifiers: chr16:g.88503796G>A (hg19) ; chr16:g.88437388G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88437388G>A , CM000678.2:g.88437388G>A	GRCh38
NC_000016.9:g.88503796G>A , CM000678.1:g.88503796G>A	GRCh37
NC_000016.8:g.87031297G>A	NCBI36
NG_012236.2:g.14918G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000565624.3:c.9918G>A MANE Select	ENSP00000456500.2:p.Arg3306=
ENST00000437464.1:c.9834G>A	ENSP00000402343.1:p.Arg3278=
ENST00000565624.1:c.9918G>A	ENSP00000456500.1:p.Arg3306=
NM_001127464.2:c.9834G>A	NP_001120936.2:p.Arg3278=
XM_011523386.1:c.9918G>A	XP_011521688.1:p.Arg3306=
XM_011523387.1:c.9918G>A	XP_011521689.1:p.Arg3306=
XM_011523388.1:c.9918G>A	XP_011521690.1:p.Arg3306=
XM_017023784.1:c.9918G>A	XP_016879273.1:p.Arg3306=
XM_017023785.1:c.9918G>A	XP_016879274.1:p.Arg3306=
NM_001367624.1:c.9918G>A	NP_001354553.1:p.Arg3306=
NM_001367624.2:c.9918G>A MANE Select	NP_001354553.1:p.Arg3306=