Canonical Allele Identifier: CA1671891533
Community Standard Title: NC_000006.12:g.149285665G=
Gene: TAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149285665G= , CM000668.2:g.149285665G= GRCh38
NC_000006.11:g.149606801G= , CM000668.1:g.149606801G= GRCh37
NC_000006.10:g.149648494G= NCBI36
NG_021386.2:g.72742G=

Transcript Alleles

HGVS Amino-acid Change
NM_001292035.2:c.6+66889G= NP_001278964.1:n.6+66889G=
NM_001292035.3:c.6+66889G= NP_001278964.1:n.6+66889G=
ENST00000606202.1:c.-121+66889G= ENSP00000476139.1:n.-121+66889G=