Canonical Allele Identifier: CA624447566
Gene: ZNF469 HGNC NCBI

Linked Data

ClinVar Variation Id: 1736903
ClinVar RCV Id: RCV002375649
dbSNP Id: rs1326657400
gnomAD v2: 16-88493876-G-A
gnomAD v3: 16-88427468-G-A
gnomAD v4: 16-88427468-G-A
MyVariant Identifiers: chr16:g.88493876G>A (hg19) chr16:g.88427468G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88427468G>A , CM000678.2:g.88427468G>A GRCh38
NC_000016.9:g.88493876G>A , CM000678.1:g.88493876G>A GRCh37
NC_000016.8:g.87021377G>A NCBI36
NG_012236.2:g.4998G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000565624.3:c.-3G>A MANE Select ENSP00000456500.2:n.-3G>A
XM_011523386.1:c.-3G>A XP_011521688.1:n.-3G>A
XM_011523387.1:c.-3G>A XP_011521689.1:n.-3G>A
XM_011523388.1:c.-3G>A XP_011521690.1:n.-3G>A
XM_017023784.1:c.-3G>A XP_016879273.1:n.-3G>A
XM_017023785.1:c.-3G>A XP_016879274.1:n.-3G>A
XR_002957934.1:n.250+2496C>T
NM_001367624.2:c.-3G>A MANE Select NP_001354553.1:n.-3G>A
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