Canonical Allele Identifier: CA1671892390
Gene: TAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149287639_149287643delinsCTCAG , CM000668.2:g.149287639_149287643delinsCTCAG GRCh38
NC_000006.11:g.149608775_149608779delinsCTCAG , CM000668.1:g.149608775_149608779delinsCTCAG GRCh37
NC_000006.10:g.149650468_149650472delinsCTCAG NCBI36
NG_021386.2:g.74716_74720delinsCTCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000606202.1:c.-121+68863_-121+68867delinsCTCAG ENSP00000476139.1:n.-121+68863_-121+68867delinsCTCAG
NM_001292035.2:c.6+68863_6+68867delinsCTCAG NP_001278964.1:n.6+68863_6+68867delinsCTCAG
NM_001292035.3:c.6+68863_6+68867delinsCTCAG NP_001278964.1:n.6+68863_6+68867delinsCTCAG