Canonical Allele Identifier: CA571322125

Gene: TAB2

Linked Data

• dbSNP Id: rs1305357273
• gnomAD v2: 6-149608763-C-CACAGGGCCGCTCTCA
• gnomAD v3: 6-149287627-C-CACAGGGCCGCTCTCA
• gnomAD v4: 6-149287627-C-CACAGGGCCGCTCTCA
• MyVariant Identifiers: chr6:g.149608763_149608764insACAGGGCCGCTCTCA (hg19) ; chr6:g.149287627_149287628insACAGGGCCGCTCTCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149287628_149287642dup , CM000668.2:g.149287628_149287642dup	GRCh38
NC_000006.11:g.149608764_149608778dup , CM000668.1:g.149608764_149608778dup	GRCh37
NC_000006.10:g.149650457_149650471dup	NCBI36
NG_021386.2:g.74705_74719dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606202.1:c.-121+68852_-121+68866dup	ENSP00000476139.1:n.-121+68852_-121+68866dup
NM_001292035.2:c.6+68852_6+68866dup	NP_001278964.1:n.6+68852_6+68866dup
NM_001292035.3:c.6+68852_6+68866dup	NP_001278964.1:n.6+68852_6+68866dup