Canonical Allele Identifier: CA2578766659

Gene: TAB2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149377989A>C , CM000668.2:g.149377989A>C	GRCh38
NC_000006.11:g.149699125A>C , CM000668.1:g.149699125A>C	GRCh37
NC_000006.10:g.149740818A>C	NCBI36
NG_021386.1:g.64690A>C
NG_021386.2:g.165066A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000703212.1:n.518-29A>C
ENST00000703213.1:c.103-29A>C	ENSP00000515239.1:n.103-29A>C
ENST00000636456.1:c.-96-683A>C	ENSP00000490379.1:n.-96-683A>C
ENST00000637181.2:c.103-29A>C MANE Select	ENSP00000490618.1:n.103-29A>C
ENST00000367456.5:c.103-29A>C	ENSP00000356426.1:n.103-29A>C
ENST00000470466.5:c.103-29A>C	ENSP00000432709.1:n.103-29A>C
ENST00000538427.5:c.103-29A>C	ENSP00000445752.1:n.103-29A>C
ENST00000606202.1:c.-120-29A>C	ENSP00000476139.1:n.-120-29A>C
NM_001292034.2:c.103-29A>C	NP_001278963.1:n.103-29A>C
NM_001292035.2:c.7-29A>C	NP_001278964.1:n.7-29A>C
NM_015093.5:c.103-29A>C	NP_055908.1:n.103-29A>C
XM_006715403.2:c.103-29A>C	XP_006715466.1:n.103-29A>C
XM_011535633.1:c.103-29A>C	XP_011533935.1:n.103-29A>C
XM_011535634.1:c.103-29A>C	XP_011533936.1:n.103-29A>C
XM_011535633.2:c.103-29A>C	XP_011533935.1:n.103-29A>C
XM_017010591.1:c.103-29A>C	XP_016866080.1:n.103-29A>C
XM_017010592.2:c.103-29A>C	XP_016866081.1:n.103-29A>C
NM_001292034.3:c.103-29A>C MANE Select	NP_001278963.1:n.103-29A>C
NM_001292035.3:c.7-29A>C	NP_001278964.1:n.7-29A>C
NM_001369506.1:c.103-29A>C	NP_001356435.1:n.103-29A>C
NM_015093.6:c.103-29A>C	NP_055908.1:n.103-29A>C