Canonical Allele Identifier: CA400050497
Gene: TBX21 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47744818C>A , CM000679.2:g.47744818C>A GRCh38
NC_000017.10:g.45822184C>A , CM000679.1:g.45822184C>A GRCh37
NC_000017.9:g.43177183C>A NCBI36
NG_012166.1:g.16575C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.1060C>A MANE Select ENSP00000177694.1:p.His354Asn
ENST00000177694.1:c.1060C>A ENSP00000177694.1:p.His354Asn
NM_013351.1:c.1060C>A NP_037483.1:p.His354Asn
XM_011524698.1:c.1123C>A XP_011523000.1:p.His375Asn
XM_011524699.1:c.727C>A XP_011523001.1:p.His243Asn
NM_013351.2:c.1060C>A MANE Select NP_037483.1:p.His354Asn