Canonical Allele Identifier: CA1671892465
Gene: TAB2 HGNC NCBI

Linked Data

dbSNP Id: rs768746251
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000606202.1:c.-121+69060C>A ENSP00000476139.1:n.-121+69060C>A
NM_001292035.2:c.6+69060C>A NP_001278964.1:n.6+69060C>A
NM_001292035.3:c.6+69060C>A NP_001278964.1:n.6+69060C>A
Search 100 bp 5'
Search 100 bp 3'