Canonical Allele Identifier: CA180680162

Gene: ZBTB10

Linked Data

• dbSNP Id: rs951486666
• gnomAD v2: 8-81438365-T-C
• gnomAD v3: 8-80526130-T-C
• gnomAD v4: 8-80526130-T-C
• MyVariant Identifiers: chr8:g.81438365T>C (hg19) ; chr8:g.80526130T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.80526130T>C , CM000670.2:g.80526130T>C	GRCh38
NC_000008.10:g.81438365T>C , CM000670.1:g.81438365T>C	GRCh37
NC_000008.9:g.81600920T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000455036.8:c.*6602T>C MANE Select	ENSP00000412036.3:n.*6602T>C
ENST00000426744.5:c.*6602T>C	ENSP00000416134.2:n.*6602T>C
ENST00000430430.5:c.*6602T>C	ENSP00000387462.1:n.*6602T>C
NM_001105539.2:c.*6602T>C	NP_001099009.1:n.*6602T>C
NM_001277145.1:c.*6602T>C	NP_001264074.1:n.*6602T>C
NM_023929.4:c.*6602T>C	NP_076418.3:n.*6602T>C
XM_005251287.3:c.*6602T>C	XP_005251344.1:n.*6602T>C
NM_001105539.3:c.*6602T>C MANE Select	NP_001099009.1:n.*6602T>C
NM_001277145.2:c.*6602T>C	NP_001264074.1:n.*6602T>C
NM_023929.5:c.*6602T>C	NP_076418.3:n.*6602T>C