Canonical Allele Identifier: CA400059877
Gene: TBX21 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733918C>G , CM000679.2:g.47733918C>G GRCh38
NC_000017.10:g.45811284C>G , CM000679.1:g.45811284C>G GRCh37
NC_000017.9:g.43166283C>G NCBI36
NG_012166.1:g.5675C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.464C>G MANE Select ENSP00000177694.1:p.Thr155Arg
ENST00000177694.1:c.464C>G ENSP00000177694.1:p.Thr155Arg
ENST00000581328.1:n.494C>G
NM_013351.1:c.464C>G NP_037483.1:p.Thr155Arg
XM_011524698.1:c.464C>G XP_011523000.1:p.Thr155Arg
NM_013351.2:c.464C>G MANE Select NP_037483.1:p.Thr155Arg