Canonical Allele Identifier: CA855801005

Gene: ZBTB10

Linked Data

• dbSNP Id: rs1214505816
• MyVariant Identifiers: chr8:g.81438463G>C (hg19) ; chr8:g.80526228G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.80526228G>C , CM000670.2:g.80526228G>C	GRCh38
NC_000008.10:g.81438463G>C , CM000670.1:g.81438463G>C	GRCh37
NC_000008.9:g.81601018G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000455036.8:c.*6700G>C MANE Select	ENSP00000412036.3:n.*6700G>C
ENST00000426744.5:c.*6700G>C	ENSP00000416134.2:n.*6700G>C
ENST00000430430.5:c.*6700G>C	ENSP00000387462.1:n.*6700G>C
NM_001105539.2:c.*6700G>C	NP_001099009.1:n.*6700G>C
NM_001277145.1:c.*6700G>C	NP_001264074.1:n.*6700G>C
NM_023929.4:c.*6700G>C	NP_076418.3:n.*6700G>C
XM_005251287.3:c.*6700G>C	XP_005251344.1:n.*6700G>C
NM_001105539.3:c.*6700G>C MANE Select	NP_001099009.1:n.*6700G>C
NM_001277145.2:c.*6700G>C	NP_001264074.1:n.*6700G>C
NM_023929.5:c.*6700G>C	NP_076418.3:n.*6700G>C