Canonical Allele Identifier: CA180680157

Gene: ZBTB10

Linked Data

• dbSNP Id: rs947265838
• MyVariant Identifiers: chr8:g.81438333A>T (hg19) ; chr8:g.80526098A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.80526098A>T , CM000670.2:g.80526098A>T	GRCh38
NC_000008.10:g.81438333A>T , CM000670.1:g.81438333A>T	GRCh37
NC_000008.9:g.81600888A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000455036.8:c.*6570A>T MANE Select	ENSP00000412036.3:n.*6570A>T
ENST00000426744.5:c.*6570A>T	ENSP00000416134.2:n.*6570A>T
ENST00000430430.5:c.*6570A>T	ENSP00000387462.1:n.*6570A>T
NM_001105539.2:c.*6570A>T	NP_001099009.1:n.*6570A>T
NM_001277145.1:c.*6570A>T	NP_001264074.1:n.*6570A>T
NM_023929.4:c.*6570A>T	NP_076418.3:n.*6570A>T
XM_005251287.3:c.*6570A>T	XP_005251344.1:n.*6570A>T
NM_001105539.3:c.*6570A>T MANE Select	NP_001099009.1:n.*6570A>T
NM_001277145.2:c.*6570A>T	NP_001264074.1:n.*6570A>T
NM_023929.5:c.*6570A>T	NP_076418.3:n.*6570A>T