Canonical Allele Identifier: CA149962313
Gene: TAB2 HGNC NCBI

Linked Data

dbSNP Id: rs545901933
gnomAD v3: 6-149287557-T-C
gnomAD v4: 6-149287557-T-C
MyVariant Identifiers: chr6:g.149608693T>C (hg19) chr6:g.149287557T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149287557T>C , CM000668.2:g.149287557T>C GRCh38
NC_000006.11:g.149608693T>C , CM000668.1:g.149608693T>C GRCh37
NC_000006.10:g.149650386T>C NCBI36
NG_021386.2:g.74634T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000606202.1:c.-121+68781T>C ENSP00000476139.1:n.-121+68781T>C
NM_001292035.2:c.6+68781T>C NP_001278964.1:n.6+68781T>C
NM_001292035.3:c.6+68781T>C NP_001278964.1:n.6+68781T>C
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