Canonical Allele Identifier: CA855800911
Gene: ZBTB10 HGNC NCBI

Linked Data

dbSNP Id: rs1274171687
MyVariant Identifiers: chr8:g.81438340G>C (hg19) chr8:g.80526105G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.80526105G>C , CM000670.2:g.80526105G>C GRCh38
NC_000008.10:g.81438340G>C , CM000670.1:g.81438340G>C GRCh37
NC_000008.9:g.81600895G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000455036.8:c.*6577G>C MANE Select ENSP00000412036.3:n.*6577G>C
ENST00000426744.5:c.*6577G>C ENSP00000416134.2:n.*6577G>C
ENST00000430430.5:c.*6577G>C ENSP00000387462.1:n.*6577G>C
NM_001105539.2:c.*6577G>C NP_001099009.1:n.*6577G>C
NM_001277145.1:c.*6577G>C NP_001264074.1:n.*6577G>C
NM_023929.4:c.*6577G>C NP_076418.3:n.*6577G>C
XM_005251287.3:c.*6577G>C XP_005251344.1:n.*6577G>C
NM_001105539.3:c.*6577G>C MANE Select NP_001099009.1:n.*6577G>C
NM_001277145.2:c.*6577G>C NP_001264074.1:n.*6577G>C
NM_023929.5:c.*6577G>C NP_076418.3:n.*6577G>C
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