Canonical Allele Identifier: CA2241069919

Gene: ZNF469

Linked Data

• dbSNP Id: rs1597205318

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88427302A>C , CM000678.2:g.88427302A>C	GRCh38
NC_000016.9:g.88493710A>C , CM000678.1:g.88493710A>C	GRCh37
NC_000016.8:g.87021211A>C	NCBI36
NG_012236.2:g.4832A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000565624.3:c.-126-43A>C MANE Select	ENSP00000456500.2:n.-126-43A>C
XM_011523386.1:c.-126-43A>C	XP_011521688.1:n.-126-43A>C
XM_011523387.1:c.-126-43A>C	XP_011521689.1:n.-126-43A>C
XM_011523388.1:c.-126-43A>C	XP_011521690.1:n.-126-43A>C
XM_017023784.1:c.-169A>C	XP_016879273.1:n.-169A>C
XM_017023785.1:c.-126-43A>C	XP_016879274.1:n.-126-43A>C
XR_002957934.1:n.250+2662T>G
NM_001367624.2:c.-126-43A>C MANE Select	NP_001354553.1:n.-126-43A>C