Canonical Allele Identifier: CA2241069930

Gene: ZNF469

Linked Data

• dbSNP Id: rs1403819638

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88427319C>T , CM000678.2:g.88427319C>T	GRCh38
NC_000016.9:g.88493727C>T , CM000678.1:g.88493727C>T	GRCh37
NC_000016.8:g.87021228C>T	NCBI36
NG_012236.2:g.4849C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000565624.3:c.-126-26C>T MANE Select	ENSP00000456500.2:n.-126-26C>T
XM_011523386.1:c.-126-26C>T	XP_011521688.1:n.-126-26C>T
XM_011523387.1:c.-126-26C>T	XP_011521689.1:n.-126-26C>T
XM_011523388.1:c.-126-26C>T	XP_011521690.1:n.-126-26C>T
XM_017023784.1:c.-152C>T	XP_016879273.1:n.-152C>T
XM_017023785.1:c.-126-26C>T	XP_016879274.1:n.-126-26C>T
XR_002957934.1:n.250+2645G>A
NM_001367624.2:c.-126-26C>T MANE Select	NP_001354553.1:n.-126-26C>T