Canonical Allele Identifier: CA1115792363
Gene: ZBTB10 HGNC NCBI

Linked Data

dbSNP Id: rs1816557687
gnomAD v3: 8-80526158-A-G
gnomAD v4: 8-80526158-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.80526158A>G , CM000670.2:g.80526158A>G GRCh38
NC_000008.10:g.81438393A>G , CM000670.1:g.81438393A>G GRCh37
NC_000008.9:g.81600948A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000455036.8:c.*6630A>G MANE Select ENSP00000412036.3:n.*6630A>G
ENST00000426744.5:c.*6630A>G ENSP00000416134.2:n.*6630A>G
ENST00000430430.5:c.*6630A>G ENSP00000387462.1:n.*6630A>G
NM_001105539.2:c.*6630A>G NP_001099009.1:n.*6630A>G
NM_001277145.1:c.*6630A>G NP_001264074.1:n.*6630A>G
NM_023929.4:c.*6630A>G NP_076418.3:n.*6630A>G
XM_005251287.3:c.*6630A>G XP_005251344.1:n.*6630A>G
NM_001105539.3:c.*6630A>G MANE Select NP_001099009.1:n.*6630A>G
NM_001277145.2:c.*6630A>G NP_001264074.1:n.*6630A>G
NM_023929.5:c.*6630A>G NP_076418.3:n.*6630A>G
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