Canonical Allele Identifier: CA571322127

Gene: TAB2

Linked Data

• dbSNP Id: rs1251431325
• gnomAD v2: 6-149608782-AGTTT-A
• gnomAD v3: 6-149287646-AGTTT-A
• gnomAD v4: 6-149287646-AGTTT-A
• MyVariant Identifiers: chr6:g.149608783_149608786del (hg19) ; chr6:g.149287647_149287650del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149287650_149287653del , CM000668.2:g.149287650_149287653del	GRCh38
NC_000006.11:g.149608786_149608789del , CM000668.1:g.149608786_149608789del	GRCh37
NC_000006.10:g.149650479_149650482del	NCBI36
NG_021386.2:g.74727_74730del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606202.1:c.-121+68874_-121+68877del	ENSP00000476139.1:n.-121+68874_-121+68877del
NM_001292035.2:c.6+68874_6+68877del	NP_001278964.1:n.6+68874_6+68877del
NM_001292035.3:c.6+68874_6+68877del	NP_001278964.1:n.6+68874_6+68877del