Canonical Allele Identifier: CA149962332

Gene: TAB2

Linked Data

• dbSNP Id: rs916421230
• MyVariant Identifiers: chr6:g.149608866C>A (hg19) ; chr6:g.149287730C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149287730C>A , CM000668.2:g.149287730C>A	GRCh38
NC_000006.11:g.149608866C>A , CM000668.1:g.149608866C>A	GRCh37
NC_000006.10:g.149650559C>A	NCBI36
NG_021386.2:g.74807C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606202.1:c.-121+68954C>A	ENSP00000476139.1:n.-121+68954C>A
NM_001292035.2:c.6+68954C>A	NP_001278964.1:n.6+68954C>A
NM_001292035.3:c.6+68954C>A	NP_001278964.1:n.6+68954C>A