Canonical Allele Identifier: CA820623852

Gene: TAB2

Linked Data

• dbSNP Id: rs1373794919
• gnomAD v3: 6-149287656-T-C
• gnomAD v4: 6-149287656-T-C
• MyVariant Identifiers: chr6:g.149608792T>C (hg19) ; chr6:g.149287656T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149287656T>C , CM000668.2:g.149287656T>C	GRCh38
NC_000006.11:g.149608792T>C , CM000668.1:g.149608792T>C	GRCh37
NC_000006.10:g.149650485T>C	NCBI36
NG_021386.2:g.74733T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606202.1:c.-121+68880T>C	ENSP00000476139.1:n.-121+68880T>C
NM_001292035.2:c.6+68880T>C	NP_001278964.1:n.6+68880T>C
NM_001292035.3:c.6+68880T>C	NP_001278964.1:n.6+68880T>C