Canonical Allele Identifier: CA452720660

Gene: TAB2

Linked Data

• MyVariant Identifiers: chr6:g.149700251C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149379115C>T , CM000668.2:g.149379115C>T	GRCh38
NC_000006.11:g.149700251C>T , CM000668.1:g.149700251C>T	GRCh37
NC_000006.10:g.149741944C>T	NCBI36
NG_021386.1:g.65816C>T
NG_021386.2:g.166192C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000703212.1:n.1615C>T
ENST00000703213.1:c.1200C>T	ENSP00000515239.1:p.Val400=
ENST00000636456.1:c.348C>T	ENSP00000490379.1:p.Val116=
ENST00000637181.2:c.1200C>T MANE Select	ENSP00000490618.1:p.Val400=
ENST00000367456.5:c.1200C>T	ENSP00000356426.1:p.Val400=
ENST00000470466.5:c.1200C>T	ENSP00000432709.1:p.Val400=
ENST00000538427.5:c.1200C>T	ENSP00000445752.1:p.Val400=
NM_001292034.2:c.1200C>T	NP_001278963.1:p.Val400=
NM_001292035.2:c.1104C>T	NP_001278964.1:p.Val368=
NM_015093.5:c.1200C>T	NP_055908.1:p.Val400=
XM_006715403.2:c.1200C>T	XP_006715466.1:p.Val400=
XM_011535633.1:c.1200C>T	XP_011533935.1:p.Val400=
XM_011535634.1:c.1200C>T	XP_011533936.1:p.Val400=
XM_011535633.2:c.1200C>T	XP_011533935.1:p.Val400=
XM_017010591.1:c.1200C>T	XP_016866080.1:p.Val400=
XM_017010592.2:c.1200C>T	XP_016866081.1:p.Val400=
NM_001292034.3:c.1200C>T MANE Select	NP_001278963.1:p.Val400=
NM_001292035.3:c.1104C>T	NP_001278964.1:p.Val368=
NM_001369506.1:c.1200C>T	NP_001356435.1:p.Val400=
NM_015093.6:c.1200C>T	NP_055908.1:p.Val400=