Canonical Allele Identifier: CA2773510237

Gene: TAB2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149287689T>C , CM000668.2:g.149287689T>C	GRCh38
NC_000006.11:g.149608825T>C , CM000668.1:g.149608825T>C	GRCh37
NC_000006.10:g.149650518T>C	NCBI36
NG_021386.2:g.74766T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000606202.1:c.-121+68913T>C	ENSP00000476139.1:n.-121+68913T>C
NM_001292035.2:c.6+68913T>C	NP_001278964.1:n.6+68913T>C
NM_001292035.3:c.6+68913T>C	NP_001278964.1:n.6+68913T>C