Canonical Allele Identifier: CA12379337

Gene: TAB2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149272784C>T , CM000668.2:g.149272784C>T	GRCh38
NC_000006.11:g.149593920C>T , CM000668.1:g.149593920C>T	GRCh37
NC_000006.10:g.149635613C>T	NCBI36
NG_021386.2:g.59861C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606202.1:c.-121+54008C>T	ENSP00000476139.1:n.-121+54008C>T
NM_001292035.2:c.6+54008C>T	NP_001278964.1:n.6+54008C>T
NM_001292035.3:c.6+54008C>T	NP_001278964.1:n.6+54008C>T