Canonical Allele Identifier: CA365994049

Gene: TAB2

Linked Data

• MyVariant Identifiers: chr6:g.149699469T>A (hg19) ; chr6:g.149378333T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149378333T>A , CM000668.2:g.149378333T>A	GRCh38
NC_000006.11:g.149699469T>A , CM000668.1:g.149699469T>A	GRCh37
NC_000006.10:g.149741162T>A	NCBI36
NG_021386.1:g.65034T>A
NG_021386.2:g.165410T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703212.1:n.833T>A
ENST00000703213.1:c.418T>A	ENSP00000515239.1:p.Phe140Ile
ENST00000636456.1:c.-96-339T>A	ENSP00000490379.1:n.-96-339T>A
ENST00000637181.2:c.418T>A MANE Select	ENSP00000490618.1:p.Phe140Ile
ENST00000367456.5:c.418T>A	ENSP00000356426.1:p.Phe140Ile
ENST00000470466.5:c.418T>A	ENSP00000432709.1:p.Phe140Ile
ENST00000538427.5:c.418T>A	ENSP00000445752.1:p.Phe140Ile
ENST00000606202.1:c.196T>A	ENSP00000476139.1:p.Phe66Ile
NM_001292034.2:c.418T>A	NP_001278963.1:p.Phe140Ile
NM_001292035.2:c.322T>A	NP_001278964.1:p.Phe108Ile
NM_015093.5:c.418T>A	NP_055908.1:p.Phe140Ile
XM_006715403.2:c.418T>A	XP_006715466.1:p.Phe140Ile
XM_011535633.1:c.418T>A	XP_011533935.1:p.Phe140Ile
XM_011535634.1:c.418T>A	XP_011533936.1:p.Phe140Ile
XM_011535633.2:c.418T>A	XP_011533935.1:p.Phe140Ile
XM_017010591.1:c.418T>A	XP_016866080.1:p.Phe140Ile
XM_017010592.2:c.418T>A	XP_016866081.1:p.Phe140Ile
NM_001292034.3:c.418T>A MANE Select	NP_001278963.1:p.Phe140Ile
NM_001292035.3:c.322T>A	NP_001278964.1:p.Phe108Ile
NM_001369506.1:c.418T>A	NP_001356435.1:p.Phe140Ile
NM_015093.6:c.418T>A	NP_055908.1:p.Phe140Ile