Canonical Allele Identifier: CA1671892396
Gene: TAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149287654A= , CM000668.2:g.149287654A= GRCh38
NC_000006.11:g.149608790A= , CM000668.1:g.149608790A= GRCh37
NC_000006.10:g.149650483A= NCBI36
NG_021386.2:g.74731A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000606202.1:c.-121+68878A= ENSP00000476139.1:n.-121+68878A=
NM_001292035.2:c.6+68878A= NP_001278964.1:n.6+68878A=
NM_001292035.3:c.6+68878A= NP_001278964.1:n.6+68878A=