Canonical Allele Identifier: CA16283199
Gene: TAB2 HGNC NCBI

Linked Data

dbSNP Id: rs76501773
gnomAD v2: 6-149608854-A-G
gnomAD v3: 6-149287718-A-G
gnomAD v4: 6-149287718-A-G
MyVariant Identifiers: chr6:g.149608854A>G (hg19) chr6:g.149287718A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149287718A>G , CM000668.2:g.149287718A>G GRCh38
NC_000006.11:g.149608854A>G , CM000668.1:g.149608854A>G GRCh37
NC_000006.10:g.149650547A>G NCBI36
NG_021386.2:g.74795A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000606202.1:c.-121+68942A>G ENSP00000476139.1:n.-121+68942A>G
NM_001292035.2:c.6+68942A>G NP_001278964.1:n.6+68942A>G
NM_001292035.3:c.6+68942A>G NP_001278964.1:n.6+68942A>G
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