Canonical Allele Identifier: CA571322126

Gene: TAB2

Linked Data

• dbSNP Id: rs1229115603
• gnomAD v2: 6-149608775-CTCAG-C
• gnomAD v3: 6-149287639-CTCAG-C
• gnomAD v4: 6-149287639-CTCAG-C
• MyVariant Identifiers: chr6:g.149608776_149608779del (hg19) ; chr6:g.149287640_149287643del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149287645_149287648del , CM000668.2:g.149287645_149287648del	GRCh38
NC_000006.11:g.149608781_149608784del , CM000668.1:g.149608781_149608784del	GRCh37
NC_000006.10:g.149650474_149650477del	NCBI36
NG_021386.2:g.74722_74725del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606202.1:c.-121+68869_-121+68872del	ENSP00000476139.1:n.-121+68869_-121+68872del
NM_001292035.2:c.6+68869_6+68872del	NP_001278964.1:n.6+68869_6+68872del
NM_001292035.3:c.6+68869_6+68872del	NP_001278964.1:n.6+68869_6+68872del