Canonical Allele Identifier: CA1796999246
Gene: ZBTB10 HGNC NCBI

Linked Data

dbSNP Id: rs1816556198

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.80526092C>G , CM000670.2:g.80526092C>G GRCh38
NC_000008.10:g.81438327C>G , CM000670.1:g.81438327C>G GRCh37
NC_000008.9:g.81600882C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000455036.8:c.*6564C>G MANE Select ENSP00000412036.3:n.*6564C>G
ENST00000426744.5:c.*6564C>G ENSP00000416134.2:n.*6564C>G
ENST00000430430.5:c.*6564C>G ENSP00000387462.1:n.*6564C>G
NM_001105539.2:c.*6564C>G NP_001099009.1:n.*6564C>G
NM_001277145.1:c.*6564C>G NP_001264074.1:n.*6564C>G
NM_023929.4:c.*6564C>G NP_076418.3:n.*6564C>G
XM_005251287.3:c.*6564C>G XP_005251344.1:n.*6564C>G
NM_001105539.3:c.*6564C>G MANE Select NP_001099009.1:n.*6564C>G
NM_001277145.2:c.*6564C>G NP_001264074.1:n.*6564C>G
NM_023929.5:c.*6564C>G NP_076418.3:n.*6564C>G