Canonical Allele Identifier: CA820623855
Gene: TAB2 HGNC NCBI

Linked Data

dbSNP Id: rs939114715
gnomAD v3: 6-149287692-A-AT
gnomAD v4: 6-149287692-A-AT
MyVariant Identifiers: chr6:g.149608828_149608829insT (hg19) chr6:g.149287692_149287693insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149287698dup , CM000668.2:g.149287698dup GRCh38
NC_000006.11:g.149608834dup , CM000668.1:g.149608834dup GRCh37
NC_000006.10:g.149650527dup NCBI36
NG_021386.2:g.74775dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000606202.1:c.-121+68922dup ENSP00000476139.1:n.-121+68922dup
NM_001292035.2:c.6+68922dup NP_001278964.1:n.6+68922dup
NM_001292035.3:c.6+68922dup NP_001278964.1:n.6+68922dup
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