Canonical Allele Identifier: CA400050582
Gene: TBX21 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47744827C>A , CM000679.2:g.47744827C>A GRCh38
NC_000017.10:g.45822193C>A , CM000679.1:g.45822193C>A GRCh37
NC_000017.9:g.43177192C>A NCBI36
NG_012166.1:g.16584C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.1069C>A MANE Select ENSP00000177694.1:p.Pro357Thr
ENST00000177694.1:c.1069C>A ENSP00000177694.1:p.Pro357Thr
NM_013351.1:c.1069C>A NP_037483.1:p.Pro357Thr
XM_011524698.1:c.1132C>A XP_011523000.1:p.Pro378Thr
XM_011524699.1:c.736C>A XP_011523001.1:p.Pro246Thr
NM_013351.2:c.1069C>A MANE Select NP_037483.1:p.Pro357Thr