Canonical Allele Identifier: CA345672208
Gene: ZBTB18 HGNC NCBI

Linked Data

ClinVar Variation Id: 225923
ClinVar RCV Id: RCV000488897 RCV002285014
dbSNP Id: rs1085307109
MyVariant Identifiers: chr1:g.244217209C>T (hg19) chr1:g.244053907C>T (hg38)
PubMed: PMID:27598823
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.244053907C>T , CM000663.2:g.244053907C>T GRCh38
NC_000001.10:g.244217209C>T , CM000663.1:g.244217209C>T GRCh37
NC_000001.9:g.242283832C>T NCBI36
NG_033841.1:g.9969C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696615.1:c.106C>T ENSP00000512755.1:p.Arg36Ter
ENST00000696616.1:c.106C>T ENSP00000512756.1:p.Arg36Ter
ENST00000696617.1:c.*63C>T ENSP00000512757.1:n.*63C>T
ENST00000696618.1:c.106C>T ENSP00000512758.1:p.Arg36Ter
ENST00000698634.1:c.106C>T ENSP00000513849.1:p.Arg36Ter
ENST00000358704.4:c.133C>T MANE Select ENSP00000351539.4:p.Arg45Ter
ENST00000622512.1:c.106C>T ENSP00000481278.1:p.Arg36Ter
NM_001278196.1:c.106C>T NP_001265125.1:p.Arg36Ter
NM_006352.4:c.106C>T NP_006343.2:p.Arg36Ter
NM_205768.2:c.133C>T NP_991331.1:p.Arg45Ter
XM_005273006.2:c.106C>T XP_005273063.1:p.Arg36Ter
XM_017000060.1:c.106C>T XP_016855549.1:p.Arg36Ter
NM_001278196.2:c.106C>T NP_001265125.1:p.Arg36Ter
NM_205768.3:c.133C>T MANE Select NP_991331.1:p.Arg45Ter
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