Canonical Allele Identifier: CA1671892440
Gene: TAB2 HGNC NCBI

Linked Data

dbSNP Id: rs1778704187

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149287778A>T , CM000668.2:g.149287778A>T GRCh38
NC_000006.11:g.149608914A>T , CM000668.1:g.149608914A>T GRCh37
NC_000006.10:g.149650607A>T NCBI36
NG_021386.2:g.74855A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000606202.1:c.-121+69002A>T ENSP00000476139.1:n.-121+69002A>T
NM_001292035.2:c.6+69002A>T NP_001278964.1:n.6+69002A>T
NM_001292035.3:c.6+69002A>T NP_001278964.1:n.6+69002A>T