Canonical Allele Identifier: CA1671892392
Gene: TAB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149287646_149287650delinsAGTTT , CM000668.2:g.149287646_149287650delinsAGTTT GRCh38
NC_000006.11:g.149608782_149608786delinsAGTTT , CM000668.1:g.149608782_149608786delinsAGTTT GRCh37
NC_000006.10:g.149650475_149650479delinsAGTTT NCBI36
NG_021386.2:g.74723_74727delinsAGTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000606202.1:c.-121+68870_-121+68874delinsAGTTT ENSP00000476139.1:n.-121+68870_-121+68874delinsAGTTT
NM_001292035.2:c.6+68870_6+68874delinsAGTTT NP_001278964.1:n.6+68870_6+68874delinsAGTTT
NM_001292035.3:c.6+68870_6+68874delinsAGTTT NP_001278964.1:n.6+68870_6+68874delinsAGTTT
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