Canonical Allele Identifier: CA16617123
Gene: ZBTB18 HGNC NCBI

Linked Data

ClinVar Variation Id: 421626
ClinVar RCV Id: RCV000478785
dbSNP Id: rs1064795259

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.244055248A>G , CM000663.2:g.244055248A>G GRCh38
NC_000001.10:g.244218550A>G , CM000663.1:g.244218550A>G GRCh37
NC_000001.9:g.242285173A>G NCBI36
NG_033841.1:g.11310A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696615.1:c.*651A>G ENSP00000512755.1:n.*651A>G
ENST00000696616.1:c.1447A>G ENSP00000512756.1:p.Arg483Gly
ENST00000696617.1:c.*1404A>G ENSP00000512757.1:n.*1404A>G
ENST00000696618.1:c.1447A>G ENSP00000512758.1:p.Arg483Gly
ENST00000358704.4:c.1474A>G MANE Select ENSP00000351539.4:p.Arg492Gly
ENST00000622512.1:c.1447A>G ENSP00000481278.1:p.Arg483Gly
NM_001278196.1:c.1447A>G NP_001265125.1:p.Arg483Gly
NM_006352.4:c.1447A>G NP_006343.2:p.Arg483Gly
NM_205768.2:c.1474A>G NP_991331.1:p.Arg492Gly
XM_005273006.2:c.1447A>G XP_005273063.1:p.Arg483Gly
XM_017000060.1:c.1447A>G XP_016855549.1:p.Arg483Gly
NM_001278196.2:c.1447A>G NP_001265125.1:p.Arg483Gly
NM_205768.3:c.1474A>G MANE Select NP_991331.1:p.Arg492Gly