Canonical Allele Identifier: CA725561718

Gene: ZNF469

Linked Data

• dbSNP Id: rs1427736720
• gnomAD v3: 16-88427334-T-C
• gnomAD v4: 16-88427334-T-C
• MyVariant Identifiers: chr16:g.88493742T>C (hg19) ; chr16:g.88427334T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88427334T>C , CM000678.2:g.88427334T>C	GRCh38
NC_000016.9:g.88493742T>C , CM000678.1:g.88493742T>C	GRCh37
NC_000016.8:g.87021243T>C	NCBI36
NG_012236.2:g.4864T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000565624.3:c.-126-11T>C MANE Select	ENSP00000456500.2:n.-126-11T>C
XM_011523386.1:c.-126-11T>C	XP_011521688.1:n.-126-11T>C
XM_011523387.1:c.-126-11T>C	XP_011521689.1:n.-126-11T>C
XM_011523388.1:c.-126-11T>C	XP_011521690.1:n.-126-11T>C
XM_017023784.1:c.-137T>C	XP_016879273.1:n.-137T>C
XM_017023785.1:c.-126-11T>C	XP_016879274.1:n.-126-11T>C
XR_002957934.1:n.250+2630A>G
NM_001367624.2:c.-126-11T>C MANE Select	NP_001354553.1:n.-126-11T>C