Canonical Allele Identifier: CA1671892363
Gene: TAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149287573T= , CM000668.2:g.149287573T= GRCh38
NC_000006.11:g.149608709T= , CM000668.1:g.149608709T= GRCh37
NC_000006.10:g.149650402T= NCBI36
NG_021386.2:g.74650T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000606202.1:c.-121+68797T= ENSP00000476139.1:n.-121+68797T=
NM_001292035.2:c.6+68797T= NP_001278964.1:n.6+68797T=
NM_001292035.3:c.6+68797T= NP_001278964.1:n.6+68797T=