Canonical Allele Identifier: CA1671892373
Gene: TAB2 HGNC NCBI

Linked Data

dbSNP Id: rs1778700615

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149287593A>T , CM000668.2:g.149287593A>T GRCh38
NC_000006.11:g.149608729A>T , CM000668.1:g.149608729A>T GRCh37
NC_000006.10:g.149650422A>T NCBI36
NG_021386.2:g.74670A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000606202.1:c.-121+68817A>T ENSP00000476139.1:n.-121+68817A>T
NM_001292035.2:c.6+68817A>T NP_001278964.1:n.6+68817A>T
NM_001292035.3:c.6+68817A>T NP_001278964.1:n.6+68817A>T