Canonical Allele Identifier: CA2241069902
Gene: ZNF469 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88427287G= , CM000678.2:g.88427287G= GRCh38
NC_000016.9:g.88493695G= , CM000678.1:g.88493695G= GRCh37
NC_000016.8:g.87021196G= NCBI36
NG_012236.2:g.4817G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000565624.3:c.-126-58G= MANE Select ENSP00000456500.2:n.-126-58G=
XM_011523386.1:c.-126-58G= XP_011521688.1:n.-126-58G=
XM_011523387.1:c.-126-58G= XP_011521689.1:n.-126-58G=
XM_011523388.1:c.-126-58G= XP_011521690.1:n.-126-58G=
XM_017023784.1:c.-184G= XP_016879273.1:n.-184G=
XM_017023785.1:c.-126-58G= XP_016879274.1:n.-126-58G=
XR_002957934.1:n.250+2677C=
NM_001367624.2:c.-126-58G= MANE Select NP_001354553.1:n.-126-58G=
Search 100 bp 5'
Search 100 bp 3'