Canonical Allele Identifier: CA12379338

Gene: TAB2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149285665G>T , CM000668.2:g.149285665G>T	GRCh38
NC_000006.11:g.149606801G>T , CM000668.1:g.149606801G>T	GRCh37
NC_000006.10:g.149648494G>T	NCBI36
NG_021386.2:g.72742G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606202.1:c.-121+66889G>T	ENSP00000476139.1:n.-121+66889G>T
NM_001292035.2:c.6+66889G>T	NP_001278964.1:n.6+66889G>T
NM_001292035.3:c.6+66889G>T	NP_001278964.1:n.6+66889G>T