Canonical Allele Identifier: CA571435648

Gene: TAB2

Linked Data

• ClinVar Variation Id: 2970595
• ClinVar RCV Id: RCV003824297
• dbSNP Id: rs1446287327
• gnomAD v2: 6-149699142-T-C
• gnomAD v3: 6-149378006-T-C
• gnomAD v4: 6-149378006-T-C
• MyVariant Identifiers: chr6:g.149699142T>C (hg19) ; chr6:g.149378006T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149378006T>C , CM000668.2:g.149378006T>C	GRCh38
NC_000006.11:g.149699142T>C , CM000668.1:g.149699142T>C	GRCh37
NC_000006.10:g.149740835T>C	NCBI36
NG_021386.1:g.64707T>C
NG_021386.2:g.165083T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000703212.1:n.518-12T>C
ENST00000703213.1:c.103-12T>C	ENSP00000515239.1:n.103-12T>C
ENST00000636456.1:c.-96-666T>C	ENSP00000490379.1:n.-96-666T>C
ENST00000637181.2:c.103-12T>C MANE Select	ENSP00000490618.1:n.103-12T>C
ENST00000367456.5:c.103-12T>C	ENSP00000356426.1:n.103-12T>C
ENST00000470466.5:c.103-12T>C	ENSP00000432709.1:n.103-12T>C
ENST00000538427.5:c.103-12T>C	ENSP00000445752.1:n.103-12T>C
ENST00000606202.1:c.-120-12T>C	ENSP00000476139.1:n.-120-12T>C
NM_001292034.2:c.103-12T>C	NP_001278963.1:n.103-12T>C
NM_001292035.2:c.7-12T>C	NP_001278964.1:n.7-12T>C
NM_015093.5:c.103-12T>C	NP_055908.1:n.103-12T>C
XM_006715403.2:c.103-12T>C	XP_006715466.1:n.103-12T>C
XM_011535633.1:c.103-12T>C	XP_011533935.1:n.103-12T>C
XM_011535634.1:c.103-12T>C	XP_011533936.1:n.103-12T>C
XM_011535633.2:c.103-12T>C	XP_011533935.1:n.103-12T>C
XM_017010591.1:c.103-12T>C	XP_016866080.1:n.103-12T>C
XM_017010592.2:c.103-12T>C	XP_016866081.1:n.103-12T>C
NM_001292034.3:c.103-12T>C MANE Select	NP_001278963.1:n.103-12T>C
NM_001292035.3:c.7-12T>C	NP_001278964.1:n.7-12T>C
NM_001369506.1:c.103-12T>C	NP_001356435.1:n.103-12T>C
NM_015093.6:c.103-12T>C	NP_055908.1:n.103-12T>C