Canonical Allele Identifier: CA1796999258
Gene: ZBTB10 HGNC NCBI

Linked Data

dbSNP Id: rs1816556711

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.80526117A>T , CM000670.2:g.80526117A>T GRCh38
NC_000008.10:g.81438352A>T , CM000670.1:g.81438352A>T GRCh37
NC_000008.9:g.81600907A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000455036.8:c.*6589A>T MANE Select ENSP00000412036.3:n.*6589A>T
ENST00000426744.5:c.*6589A>T ENSP00000416134.2:n.*6589A>T
ENST00000430430.5:c.*6589A>T ENSP00000387462.1:n.*6589A>T
NM_001105539.2:c.*6589A>T NP_001099009.1:n.*6589A>T
NM_001277145.1:c.*6589A>T NP_001264074.1:n.*6589A>T
NM_023929.4:c.*6589A>T NP_076418.3:n.*6589A>T
XM_005251287.3:c.*6589A>T XP_005251344.1:n.*6589A>T
NM_001105539.3:c.*6589A>T MANE Select NP_001099009.1:n.*6589A>T
NM_001277145.2:c.*6589A>T NP_001264074.1:n.*6589A>T
NM_023929.5:c.*6589A>T NP_076418.3:n.*6589A>T