Canonical Allele Identifier: CA2580593681
Gene: TAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149287738G>T , CM000668.2:g.149287738G>T GRCh38
NC_000006.11:g.149608874G>T , CM000668.1:g.149608874G>T GRCh37
NC_000006.10:g.149650567G>T NCBI36
NG_021386.2:g.74815G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000606202.1:c.-121+68962G>T ENSP00000476139.1:n.-121+68962G>T
NM_001292035.2:c.6+68962G>T NP_001278964.1:n.6+68962G>T
NM_001292035.3:c.6+68962G>T NP_001278964.1:n.6+68962G>T