Canonical Allele Identifier: CA1095712590
Gene: TAB2 HGNC NCBI

Linked Data

dbSNP Id: rs1778704116
gnomAD v3: 6-149287773-G-A
gnomAD v4: 6-149287773-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149287773G>A , CM000668.2:g.149287773G>A GRCh38
NC_000006.11:g.149608909G>A , CM000668.1:g.149608909G>A GRCh37
NC_000006.10:g.149650602G>A NCBI36
NG_021386.2:g.74850G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000606202.1:c.-121+68997G>A ENSP00000476139.1:n.-121+68997G>A
NM_001292035.2:c.6+68997G>A NP_001278964.1:n.6+68997G>A
NM_001292035.3:c.6+68997G>A NP_001278964.1:n.6+68997G>A
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