Canonical Allele Identifier: CA1671892376
Gene: TAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149287597A= , CM000668.2:g.149287597A= GRCh38
NC_000006.11:g.149608733A= , CM000668.1:g.149608733A= GRCh37
NC_000006.10:g.149650426A= NCBI36
NG_021386.2:g.74674A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000606202.1:c.-121+68821A= ENSP00000476139.1:n.-121+68821A=
NM_001292035.2:c.6+68821A= NP_001278964.1:n.6+68821A=
NM_001292035.3:c.6+68821A= NP_001278964.1:n.6+68821A=