Canonical Allele Identifier: CA1671881107
Community Standard Title: NC_000006.12:g.149272784C=
Gene: TAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149272784C= , CM000668.2:g.149272784C= GRCh38
NC_000006.11:g.149593920C= , CM000668.1:g.149593920C= GRCh37
NC_000006.10:g.149635613C= NCBI36
NG_021386.2:g.59861C=

Transcript Alleles

HGVS Amino-acid Change
NM_001292035.2:c.6+54008C= NP_001278964.1:n.6+54008C=
NM_001292035.3:c.6+54008C= NP_001278964.1:n.6+54008C=
ENST00000606202.1:c.-121+54008C= ENSP00000476139.1:n.-121+54008C=