Canonical Allele Identifier: CA2262805673
Gene: TBX21 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733557T= , CM000679.2:g.47733557T= GRCh38
NC_000017.10:g.45810923T= , CM000679.1:g.45810923T= GRCh37
NC_000017.9:g.43165922T= NCBI36
NG_012166.1:g.5314T=

Transcript Alleles

HGVS Amino-acid change
ENST00000177694.2:c.103T= MANE Select ENSP00000177694.1:p.Tyr35=
ENST00000177694.1:c.103T= ENSP00000177694.1:p.Tyr35=
ENST00000581328.1:n.133T=
NM_013351.1:c.103T= NP_037483.1:p.Tyr35=
XM_011524698.1:c.103T= XP_011523000.1:p.Tyr35=
NM_013351.2:c.103T= MANE Select NP_037483.1:p.Tyr35=