Canonical Allele Identifier: CA149962333
Gene: TAB2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs9485372

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149287738G>A , CM000668.2:g.149287738G>A GRCh38
NC_000006.11:g.149608874G>A , CM000668.1:g.149608874G>A GRCh37
NC_000006.10:g.149650567G>A NCBI36
NG_021386.2:g.74815G>A

Transcript Alleles

HGVS Amino-acid change
NM_001292035.2:c.6+68962G>A VV NP_001278964.1:p.=
ENST00000606202.1:c.-121+68962G>A ENSP00000476139.1:p.=