Canonical Allele Identifier: CA149962320

Gene: TAB2

Linked Data

• dbSNP Id: rs772411908
• gnomAD v2: 6-149608737-A-G
• gnomAD v3: 6-149287601-A-G
• gnomAD v4: 6-149287601-A-G
• MyVariant Identifiers: chr6:g.149608737A>G (hg19) ; chr6:g.149287601A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149287601A>G , CM000668.2:g.149287601A>G	GRCh38
NC_000006.11:g.149608737A>G , CM000668.1:g.149608737A>G	GRCh37
NC_000006.10:g.149650430A>G	NCBI36
NG_021386.2:g.74678A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606202.1:c.-121+68825A>G	ENSP00000476139.1:n.-121+68825A>G
NM_001292035.2:c.6+68825A>G	NP_001278964.1:n.6+68825A>G
NM_001292035.3:c.6+68825A>G	NP_001278964.1:n.6+68825A>G