Canonical Allele Identifier: CA1095712582

Gene: TAB2

Linked Data

• dbSNP Id: rs1778703023
• gnomAD v3: 6-149287720-A-G
• gnomAD v4: 6-149287720-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149287720A>G , CM000668.2:g.149287720A>G	GRCh38
NC_000006.11:g.149608856A>G , CM000668.1:g.149608856A>G	GRCh37
NC_000006.10:g.149650549A>G	NCBI36
NG_021386.2:g.74797A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000606202.1:c.-121+68944A>G	ENSP00000476139.1:n.-121+68944A>G
NM_001292035.2:c.6+68944A>G	NP_001278964.1:n.6+68944A>G
NM_001292035.3:c.6+68944A>G	NP_001278964.1:n.6+68944A>G