Canonical Allele Identifier: CA400059332
Gene: TBX21 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733849A>C , CM000679.2:g.47733849A>C GRCh38
NC_000017.10:g.45811215A>C , CM000679.1:g.45811215A>C GRCh37
NC_000017.9:g.43166214A>C NCBI36
NG_012166.1:g.5606A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.395A>C MANE Select ENSP00000177694.1:p.Glu132Ala
ENST00000177694.1:c.395A>C ENSP00000177694.1:p.Glu132Ala
ENST00000581328.1:n.425A>C
NM_013351.1:c.395A>C NP_037483.1:p.Glu132Ala
XM_011524698.1:c.395A>C XP_011523000.1:p.Glu132Ala
NM_013351.2:c.395A>C MANE Select NP_037483.1:p.Glu132Ala