Canonical Allele Identifier: CA2773510235
Gene: TAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149287611dup , CM000668.2:g.149287611dup GRCh38
NC_000006.11:g.149608747dup , CM000668.1:g.149608747dup GRCh37
NC_000006.10:g.149650440dup NCBI36
NG_021386.2:g.74688dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000606202.1:c.-121+68835dup ENSP00000476139.1:n.-121+68835dup
NM_001292035.2:c.6+68835dup NP_001278964.1:n.6+68835dup
NM_001292035.3:c.6+68835dup NP_001278964.1:n.6+68835dup