Canonical Allele Identifier: CA571322124

Gene: TAB2

Linked Data

• dbSNP Id: rs1247098475
• gnomAD v2: 6-149608735-A-G
• MyVariant Identifiers: chr6:g.149608735A>G (hg19) ; chr6:g.149287599A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149287599A>G , CM000668.2:g.149287599A>G	GRCh38
NC_000006.11:g.149608735A>G , CM000668.1:g.149608735A>G	GRCh37
NC_000006.10:g.149650428A>G	NCBI36
NG_021386.2:g.74676A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606202.1:c.-121+68823A>G	ENSP00000476139.1:n.-121+68823A>G
NM_001292035.2:c.6+68823A>G	NP_001278964.1:n.6+68823A>G
NM_001292035.3:c.6+68823A>G	NP_001278964.1:n.6+68823A>G