Canonical Allele Identifier: CA397125361
Gene: ZNF469 HGNC NCBI

Linked Data

dbSNP Id: rs1206417002

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88437447C>T , CM000678.2:g.88437447C>T GRCh38
NC_000016.9:g.88503855C>T , CM000678.1:g.88503855C>T GRCh37
NC_000016.8:g.87031356C>T NCBI36
NG_012236.2:g.14977C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000565624.3:c.9977C>T MANE Select ENSP00000456500.2:p.Thr3326Ile
ENST00000437464.1:c.9893C>T ENSP00000402343.1:p.Thr3298Ile
ENST00000565624.1:c.9977C>T ENSP00000456500.1:p.Thr3326Ile
NM_001127464.2:c.9893C>T NP_001120936.2:p.Thr3298Ile
XM_011523386.1:c.9977C>T XP_011521688.1:p.Thr3326Ile
XM_011523387.1:c.9977C>T XP_011521689.1:p.Thr3326Ile
XM_011523388.1:c.9977C>T XP_011521690.1:p.Thr3326Ile
XM_017023784.1:c.9977C>T XP_016879273.1:p.Thr3326Ile
XM_017023785.1:c.9977C>T XP_016879274.1:p.Thr3326Ile
NM_001367624.1:c.9977C>T NP_001354553.1:p.Thr3326Ile
NM_001367624.2:c.9977C>T MANE Select NP_001354553.1:p.Thr3326Ile