Canonical Allele Identifier: CA149962337
Gene: TAB2 HGNC NCBI

Linked Data

dbSNP Id: rs952784443
MyVariant Identifiers: chr6:g.149608925T>A (hg19) chr6:g.149287789T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149287789T>A , CM000668.2:g.149287789T>A GRCh38
NC_000006.11:g.149608925T>A , CM000668.1:g.149608925T>A GRCh37
NC_000006.10:g.149650618T>A NCBI36
NG_021386.2:g.74866T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000606202.1:c.-121+69013T>A ENSP00000476139.1:n.-121+69013T>A
NM_001292035.2:c.6+69013T>A NP_001278964.1:n.6+69013T>A
NM_001292035.3:c.6+69013T>A NP_001278964.1:n.6+69013T>A
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