Canonical Allele Identifier: CA123071
Gene: ZBTB16 HGNC NCBI

Linked Data

ClinVar Variation Id: 13376
ClinVar RCV Id: RCV000014305
dbSNP Id: rs121434606
MyVariant Identifiers: chr11:g.114121104A>G (hg19) chr11:g.114250382A>G (hg38)
PubMed: PMID:11891687 PMID:18611983
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.114250382A>G , CM000673.2:g.114250382A>G GRCh38
NC_000011.9:g.114121104A>G , CM000673.1:g.114121104A>G GRCh37
NC_000011.8:g.113626314A>G NCBI36
NG_012140.1:g.195674A>G
NG_012140.2:g.195807A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000682218.1:n.2506A>G
ENST00000682278.1:c.1849A>G ENSP00000506794.1:p.Met617Val
ENST00000682697.1:c.1849A>G ENSP00000506924.1:p.Met617Val
ENST00000682810.1:c.1762A>G ENSP00000507219.1:p.Met588Val
ENST00000682971.1:c.1849A>G ENSP00000506894.1:p.Met617Val
ENST00000683006.1:n.546A>G
ENST00000683233.1:c.*389A>G ENSP00000506995.1:n.*389A>G
ENST00000683318.1:c.1849A>G ENSP00000508351.1:p.Met617Val
ENST00000683554.1:c.1849A>G ENSP00000506953.1:p.Met617Val
ENST00000684295.1:c.1849A>G ENSP00000507788.1:p.Met617Val
ENST00000684612.1:c.1921A>G ENSP00000507350.1:p.Met641Val
ENST00000335953.9:c.1849A>G MANE Select ENSP00000338157.4:p.Met617Val
ENST00000335953.8:c.1849A>G ENSP00000338157.4:p.Met617Val
ENST00000392996.2:c.1849A>G ENSP00000376721.2:p.Met617Val
ENST00000535379.1:n.530A>G
ENST00000535509.1:n.633A>G
NM_001018011.1:c.1849A>G NP_001018011.1:p.Met617Val
NM_006006.4:c.1849A>G NP_005997.2:p.Met617Val
NM_001018011.2:c.1849A>G NP_001018011.1:p.Met617Val
NM_001354750.1:c.1849A>G NP_001341679.1:p.Met617Val
NM_001354751.1:c.1849A>G NP_001341680.1:p.Met617Val
NM_001354752.1:c.1762A>G NP_001341681.1:p.Met588Val
NM_006006.5:c.1849A>G NP_005997.2:p.Met617Val
XM_017018259.1:c.1849A>G XP_016873748.1:p.Met617Val
NM_001354750.2:c.1849A>G NP_001341679.1:p.Met617Val
NM_001354751.2:c.1849A>G NP_001341680.1:p.Met617Val
NM_006006.6:c.1849A>G MANE Select NP_005997.2:p.Met617Val
NM_001018011.3:c.1849A>G NP_001018011.1:p.Met617Val
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