Canonical Allele Identifier: CA149962318

Gene: TAB2

Linked Data

• dbSNP Id: rs1010632554
• MyVariant Identifiers: chr6:g.149608732T>A (hg19) ; chr6:g.149287596T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149287596T>A , CM000668.2:g.149287596T>A	GRCh38
NC_000006.11:g.149608732T>A , CM000668.1:g.149608732T>A	GRCh37
NC_000006.10:g.149650425T>A	NCBI36
NG_021386.2:g.74673T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606202.1:c.-121+68820T>A	ENSP00000476139.1:n.-121+68820T>A
NM_001292035.2:c.6+68820T>A	NP_001278964.1:n.6+68820T>A
NM_001292035.3:c.6+68820T>A	NP_001278964.1:n.6+68820T>A