Canonical Allele Identifier: CA1671892464
Gene: TAB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149287836C= , CM000668.2:g.149287836C= GRCh38
NC_000006.11:g.149608972C= , CM000668.1:g.149608972C= GRCh37
NC_000006.10:g.149650665C= NCBI36
NG_021386.2:g.74913C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000606202.1:c.-121+69060C= ENSP00000476139.1:n.-121+69060C=
NM_001292035.2:c.6+69060C= NP_001278964.1:n.6+69060C=
NM_001292035.3:c.6+69060C= NP_001278964.1:n.6+69060C=
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