Canonical Allele Identifier: CA452719825

Gene: TAB2

Linked Data

• dbSNP Id: rs1781477171
• MyVariant Identifiers: chr6:g.149699468T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149378332T>G , CM000668.2:g.149378332T>G	GRCh38
NC_000006.11:g.149699468T>G , CM000668.1:g.149699468T>G	GRCh37
NC_000006.10:g.149741161T>G	NCBI36
NG_021386.1:g.65033T>G
NG_021386.2:g.165409T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703212.1:n.832T>G
ENST00000703213.1:c.417T>G	ENSP00000515239.1:p.Val139=
ENST00000636456.1:c.-96-340T>G	ENSP00000490379.1:n.-96-340T>G
ENST00000637181.2:c.417T>G MANE Select	ENSP00000490618.1:p.Val139=
ENST00000367456.5:c.417T>G	ENSP00000356426.1:p.Val139=
ENST00000470466.5:c.417T>G	ENSP00000432709.1:p.Val139=
ENST00000538427.5:c.417T>G	ENSP00000445752.1:p.Val139=
ENST00000606202.1:c.195T>G	ENSP00000476139.1:p.Val65=
NM_001292034.2:c.417T>G	NP_001278963.1:p.Val139=
NM_001292035.2:c.321T>G	NP_001278964.1:p.Val107=
NM_015093.5:c.417T>G	NP_055908.1:p.Val139=
XM_006715403.2:c.417T>G	XP_006715466.1:p.Val139=
XM_011535633.1:c.417T>G	XP_011533935.1:p.Val139=
XM_011535634.1:c.417T>G	XP_011533936.1:p.Val139=
XM_011535633.2:c.417T>G	XP_011533935.1:p.Val139=
XM_017010591.1:c.417T>G	XP_016866080.1:p.Val139=
XM_017010592.2:c.417T>G	XP_016866081.1:p.Val139=
NM_001292034.3:c.417T>G MANE Select	NP_001278963.1:p.Val139=
NM_001292035.3:c.321T>G	NP_001278964.1:p.Val107=
NM_001369506.1:c.417T>G	NP_001356435.1:p.Val139=
NM_015093.6:c.417T>G	NP_055908.1:p.Val139=