Canonical Allele Identifier: CA2638460617
Gene: TBX21 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733756del , CM000679.2:g.47733756del GRCh38
NC_000017.10:g.45811122del , CM000679.1:g.45811122del GRCh37
NC_000017.9:g.43166121del NCBI36
NG_012166.1:g.5513del

Transcript Alleles

HGVS Amino-acid change
ENST00000177694.2:c.302del MANE Select ENSP00000177694.1:p.Gly101AlafsTer?
ENST00000177694.1:c.302del ENSP00000177694.1:p.Gly101AlafsTer?
ENST00000581328.1:n.332del
NM_013351.1:c.302del NP_037483.1:p.Gly101AlafsTer?
XM_011524698.1:c.302del XP_011523000.1:p.Gly101AlafsTer?
NM_013351.2:c.302del MANE Select NP_037483.1:p.Gly101AlafsTer?