Canonical Allele Identifier: CA820623892

Gene: TAB2

Linked Data

• dbSNP Id: rs1271247242
• MyVariant Identifiers: chr6:g.149609005T>G (hg19) ; chr6:g.149287869T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149287869T>G , CM000668.2:g.149287869T>G	GRCh38
NC_000006.11:g.149609005T>G , CM000668.1:g.149609005T>G	GRCh37
NC_000006.10:g.149650698T>G	NCBI36
NG_021386.2:g.74946T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606202.1:c.-121+69093T>G	ENSP00000476139.1:n.-121+69093T>G
NM_001292035.2:c.6+69093T>G	NP_001278964.1:n.6+69093T>G
NM_001292035.3:c.6+69093T>G	NP_001278964.1:n.6+69093T>G