Canonical Allele Identifier: CA2634823918

Gene: ZNF469

Linked Data

• gnomAD v4: 16-88427320-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88427320A>C , CM000678.2:g.88427320A>C	GRCh38
NC_000016.9:g.88493728A>C , CM000678.1:g.88493728A>C	GRCh37
NC_000016.8:g.87021229A>C	NCBI36
NG_012236.2:g.4850A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000565624.3:c.-126-25A>C MANE Select	ENSP00000456500.2:n.-126-25A>C
XM_011523386.1:c.-126-25A>C	XP_011521688.1:n.-126-25A>C
XM_011523387.1:c.-126-25A>C	XP_011521689.1:n.-126-25A>C
XM_011523388.1:c.-126-25A>C	XP_011521690.1:n.-126-25A>C
XM_017023784.1:c.-151A>C	XP_016879273.1:n.-151A>C
XM_017023785.1:c.-126-25A>C	XP_016879274.1:n.-126-25A>C
XR_002957934.1:n.250+2644T>G
NM_001367624.2:c.-126-25A>C MANE Select	NP_001354553.1:n.-126-25A>C