Canonical Allele Identifier: CA4041363

Gene: TAB2

Linked Data

• dbSNP Id: rs768728365
• ExAC: 6:149699219 T / C
• gnomAD v2: 6-149699219-T-C
• gnomAD v3: 6-149378083-T-C
• gnomAD v4: 6-149378083-T-C
• MyVariant Identifiers: chr6:g.149699219T>C (hg19) ; chr6:g.149378083T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149378083T>C , CM000668.2:g.149378083T>C	GRCh38
NC_000006.11:g.149699219T>C , CM000668.1:g.149699219T>C	GRCh37
NC_000006.10:g.149740912T>C	NCBI36
NG_021386.1:g.64784T>C
NG_021386.2:g.165160T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703212.1:n.583T>C
ENST00000703213.1:c.168T>C	ENSP00000515239.1:p.Gly56=
ENST00000636456.1:c.-96-589T>C	ENSP00000490379.1:n.-96-589T>C
ENST00000637181.2:c.168T>C MANE Select	ENSP00000490618.1:p.Gly56=
ENST00000367456.5:c.168T>C	ENSP00000356426.1:p.Gly56=
ENST00000470466.5:c.168T>C	ENSP00000432709.1:p.Gly56=
ENST00000538427.5:c.168T>C	ENSP00000445752.1:p.Gly56=
ENST00000606202.1:c.-55T>C	ENSP00000476139.1:n.-55T>C
NM_001292034.2:c.168T>C	NP_001278963.1:p.Gly56=
NM_001292035.2:c.72T>C	NP_001278964.1:p.Gly24=
NM_015093.5:c.168T>C	NP_055908.1:p.Gly56=
XM_006715403.2:c.168T>C	XP_006715466.1:p.Gly56=
XM_011535633.1:c.168T>C	XP_011533935.1:p.Gly56=
XM_011535634.1:c.168T>C	XP_011533936.1:p.Gly56=
XM_011535633.2:c.168T>C	XP_011533935.1:p.Gly56=
XM_017010591.1:c.168T>C	XP_016866080.1:p.Gly56=
XM_017010592.2:c.168T>C	XP_016866081.1:p.Gly56=
NM_001292034.3:c.168T>C MANE Select	NP_001278963.1:p.Gly56=
NM_001292035.3:c.72T>C	NP_001278964.1:p.Gly24=
NM_001369506.1:c.168T>C	NP_001356435.1:p.Gly56=
NM_015093.6:c.168T>C	NP_055908.1:p.Gly56=