Canonical Allele Identifier: CA1671892419

Gene: TAB2

Linked Data

• dbSNP Id: rs1778702698

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149287712A>T , CM000668.2:g.149287712A>T	GRCh38
NC_000006.11:g.149608848A>T , CM000668.1:g.149608848A>T	GRCh37
NC_000006.10:g.149650541A>T	NCBI36
NG_021386.2:g.74789A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000606202.1:c.-121+68936A>T	ENSP00000476139.1:n.-121+68936A>T
NM_001292035.2:c.6+68936A>T	NP_001278964.1:n.6+68936A>T
NM_001292035.3:c.6+68936A>T	NP_001278964.1:n.6+68936A>T