Canonical Allele Identifier: CA452719817

Gene: TAB2

Linked Data

• MyVariant Identifiers: chr6:g.149699459C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149378323C>A , CM000668.2:g.149378323C>A	GRCh38
NC_000006.11:g.149699459C>A , CM000668.1:g.149699459C>A	GRCh37
NC_000006.10:g.149741152C>A	NCBI36
NG_021386.1:g.65024C>A
NG_021386.2:g.165400C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000703212.1:n.823C>A
ENST00000703213.1:c.408C>A	ENSP00000515239.1:p.Gly136=
ENST00000636456.1:c.-96-349C>A	ENSP00000490379.1:n.-96-349C>A
ENST00000637181.2:c.408C>A MANE Select	ENSP00000490618.1:p.Gly136=
ENST00000367456.5:c.408C>A	ENSP00000356426.1:p.Gly136=
ENST00000470466.5:c.408C>A	ENSP00000432709.1:p.Gly136=
ENST00000538427.5:c.408C>A	ENSP00000445752.1:p.Gly136=
ENST00000606202.1:c.186C>A	ENSP00000476139.1:p.Gly62=
NM_001292034.2:c.408C>A	NP_001278963.1:p.Gly136=
NM_001292035.2:c.312C>A	NP_001278964.1:p.Gly104=
NM_015093.5:c.408C>A	NP_055908.1:p.Gly136=
XM_006715403.2:c.408C>A	XP_006715466.1:p.Gly136=
XM_011535633.1:c.408C>A	XP_011533935.1:p.Gly136=
XM_011535634.1:c.408C>A	XP_011533936.1:p.Gly136=
XM_011535633.2:c.408C>A	XP_011533935.1:p.Gly136=
XM_017010591.1:c.408C>A	XP_016866080.1:p.Gly136=
XM_017010592.2:c.408C>A	XP_016866081.1:p.Gly136=
NM_001292034.3:c.408C>A MANE Select	NP_001278963.1:p.Gly136=
NM_001292035.3:c.312C>A	NP_001278964.1:p.Gly104=
NM_001369506.1:c.408C>A	NP_001356435.1:p.Gly136=
NM_015093.6:c.408C>A	NP_055908.1:p.Gly136=