Canonical Allele Identifier: CA571322132
Gene: TAB2 HGNC NCBI

Linked Data

dbSNP Id: rs1469295255
gnomAD v2: 6-149608945-G-A
gnomAD v3: 6-149287809-G-A
gnomAD v4: 6-149287809-G-A
MyVariant Identifiers: chr6:g.149608945G>A (hg19) chr6:g.149287809G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149287809G>A , CM000668.2:g.149287809G>A GRCh38
NC_000006.11:g.149608945G>A , CM000668.1:g.149608945G>A GRCh37
NC_000006.10:g.149650638G>A NCBI36
NG_021386.2:g.74886G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000606202.1:c.-121+69033G>A ENSP00000476139.1:n.-121+69033G>A
NM_001292035.2:c.6+69033G>A NP_001278964.1:n.6+69033G>A
NM_001292035.3:c.6+69033G>A NP_001278964.1:n.6+69033G>A
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