Canonical Allele Identifier: CA149916039

Gene: TAB2

Linked Data

• dbSNP Id: rs951108891
• gnomAD v3: 6-149378338-A-T
• gnomAD v4: 6-149378338-A-T
• MyVariant Identifiers: chr6:g.149699474A>T (hg19) ; chr6:g.149378338A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149378338A>T , CM000668.2:g.149378338A>T	GRCh38
NC_000006.11:g.149699474A>T , CM000668.1:g.149699474A>T	GRCh37
NC_000006.10:g.149741167A>T	NCBI36
NG_021386.1:g.65039A>T
NG_021386.2:g.165415A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000703212.1:n.838A>T
ENST00000703213.1:c.423A>T	ENSP00000515239.1:p.Gly141=
ENST00000636456.1:c.-96-334A>T	ENSP00000490379.1:n.-96-334A>T
ENST00000637181.2:c.423A>T MANE Select	ENSP00000490618.1:p.Gly141=
ENST00000367456.5:c.423A>T	ENSP00000356426.1:p.Gly141=
ENST00000470466.5:c.423A>T	ENSP00000432709.1:p.Gly141=
ENST00000538427.5:c.423A>T	ENSP00000445752.1:p.Gly141=
ENST00000606202.1:c.201A>T	ENSP00000476139.1:p.Gly67=
NM_001292034.2:c.423A>T	NP_001278963.1:p.Gly141=
NM_001292035.2:c.327A>T	NP_001278964.1:p.Gly109=
NM_015093.5:c.423A>T	NP_055908.1:p.Gly141=
XM_006715403.2:c.423A>T	XP_006715466.1:p.Gly141=
XM_011535633.1:c.423A>T	XP_011533935.1:p.Gly141=
XM_011535634.1:c.423A>T	XP_011533936.1:p.Gly141=
XM_011535633.2:c.423A>T	XP_011533935.1:p.Gly141=
XM_017010591.1:c.423A>T	XP_016866080.1:p.Gly141=
XM_017010592.2:c.423A>T	XP_016866081.1:p.Gly141=
NM_001292034.3:c.423A>T MANE Select	NP_001278963.1:p.Gly141=
NM_001292035.3:c.327A>T	NP_001278964.1:p.Gly109=
NM_001369506.1:c.423A>T	NP_001356435.1:p.Gly141=
NM_015093.6:c.423A>T	NP_055908.1:p.Gly141=