Canonical Allele Identifier: CA571322131
Gene: TAB2 HGNC NCBI

Linked Data

gnomAD v2: 6-149608938-C-T
MyVariant Identifiers: chr6:g.149608938C>T (hg19) chr6:g.149287802C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149287802C>T , CM000668.2:g.149287802C>T GRCh38
NC_000006.11:g.149608938C>T , CM000668.1:g.149608938C>T GRCh37
NC_000006.10:g.149650631C>T NCBI36
NG_021386.2:g.74879C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000606202.1:c.-121+69026C>T ENSP00000476139.1:n.-121+69026C>T
NM_001292035.2:c.6+69026C>T NP_001278964.1:n.6+69026C>T
NM_001292035.3:c.6+69026C>T NP_001278964.1:n.6+69026C>T
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