Canonical Allele Identifier: CA2262805626
Gene: TBX21 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733480G= , CM000679.2:g.47733480G= GRCh38
NC_000017.10:g.45810846G= , CM000679.1:g.45810846G= GRCh37
NC_000017.9:g.43165845G= NCBI36
NG_012166.1:g.5237G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.26G= MANE Select ENSP00000177694.1:p.Gly9=
ENST00000177694.1:c.26G= ENSP00000177694.1:p.Gly9=
ENST00000581328.1:n.56G=
NM_013351.1:c.26G= NP_037483.1:p.Gly9=
XM_011524698.1:c.26G= XP_011523000.1:p.Gly9=
NM_013351.2:c.26G= MANE Select NP_037483.1:p.Gly9=