Canonical Allele Identifier: CA855800902
Gene: ZBTB10 HGNC NCBI

Linked Data

dbSNP Id: rs1270945415
gnomAD v3: 8-80526094-T-A
gnomAD v4: 8-80526094-T-A
MyVariant Identifiers: chr8:g.81438329T>A (hg19) chr8:g.80526094T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.80526094T>A , CM000670.2:g.80526094T>A GRCh38
NC_000008.10:g.81438329T>A , CM000670.1:g.81438329T>A GRCh37
NC_000008.9:g.81600884T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000455036.8:c.*6566T>A MANE Select ENSP00000412036.3:n.*6566T>A
ENST00000426744.5:c.*6566T>A ENSP00000416134.2:n.*6566T>A
ENST00000430430.5:c.*6566T>A ENSP00000387462.1:n.*6566T>A
NM_001105539.2:c.*6566T>A NP_001099009.1:n.*6566T>A
NM_001277145.1:c.*6566T>A NP_001264074.1:n.*6566T>A
NM_023929.4:c.*6566T>A NP_076418.3:n.*6566T>A
XM_005251287.3:c.*6566T>A XP_005251344.1:n.*6566T>A
NM_001105539.3:c.*6566T>A MANE Select NP_001099009.1:n.*6566T>A
NM_001277145.2:c.*6566T>A NP_001264074.1:n.*6566T>A
NM_023929.5:c.*6566T>A NP_076418.3:n.*6566T>A
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