Canonical Allele Identifier: CA1671892490
Gene: TAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149287881C= , CM000668.2:g.149287881C= GRCh38
NC_000006.11:g.149609017C= , CM000668.1:g.149609017C= GRCh37
NC_000006.10:g.149650710C= NCBI36
NG_021386.2:g.74958C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000606202.1:c.-121+69105C= ENSP00000476139.1:n.-121+69105C=
NM_001292035.2:c.6+69105C= NP_001278964.1:n.6+69105C=
NM_001292035.3:c.6+69105C= NP_001278964.1:n.6+69105C=