Canonical Allele Identifier: CA397125062

Gene: ZNF469

Linked Data

• ClinVar Variation Id: 2683382
• ClinVar RCV Id: RCV003480202
• dbSNP Id: rs1472267071
• gnomAD v3: 16-88437372-G-T
• gnomAD v4: 16-88437372-G-T
• MyVariant Identifiers: chr16:g.88503780G>T (hg19) ; chr16:g.88437372G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88437372G>T , CM000678.2:g.88437372G>T	GRCh38
NC_000016.9:g.88503780G>T , CM000678.1:g.88503780G>T	GRCh37
NC_000016.8:g.87031281G>T	NCBI36
NG_012236.2:g.14902G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000565624.3:c.9902G>T MANE Select	ENSP00000456500.2:p.Ser3301Ile
ENST00000437464.1:c.9818G>T	ENSP00000402343.1:p.Ser3273Ile
ENST00000565624.1:c.9902G>T	ENSP00000456500.1:p.Ser3301Ile
NM_001127464.2:c.9818G>T	NP_001120936.2:p.Ser3273Ile
XM_011523386.1:c.9902G>T	XP_011521688.1:p.Ser3301Ile
XM_011523387.1:c.9902G>T	XP_011521689.1:p.Ser3301Ile
XM_011523388.1:c.9902G>T	XP_011521690.1:p.Ser3301Ile
XM_017023784.1:c.9902G>T	XP_016879273.1:p.Ser3301Ile
XM_017023785.1:c.9902G>T	XP_016879274.1:p.Ser3301Ile
NM_001367624.1:c.9902G>T	NP_001354553.1:p.Ser3301Ile
NM_001367624.2:c.9902G>T MANE Select	NP_001354553.1:p.Ser3301Ile