Canonical Allele Identifier: CA1671892412
Gene: TAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149287692_149287693delinsAT , CM000668.2:g.149287692_149287693delinsAT GRCh38
NC_000006.11:g.149608828_149608829delinsAT , CM000668.1:g.149608828_149608829delinsAT GRCh37
NC_000006.10:g.149650521_149650522delinsAT NCBI36
NG_021386.2:g.74769_74770delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000606202.1:c.-121+68916_-121+68917delinsAT ENSP00000476139.1:n.-121+68916_-121+68917delinsAT
NM_001292035.2:c.6+68916_6+68917delinsAT NP_001278964.1:n.6+68916_6+68917delinsAT
NM_001292035.3:c.6+68916_6+68917delinsAT NP_001278964.1:n.6+68916_6+68917delinsAT