Canonical Allele Identifier: CA400058773
Gene: TBX21 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733732T>G , CM000679.2:g.47733732T>G GRCh38
NC_000017.10:g.45811098T>G , CM000679.1:g.45811098T>G GRCh37
NC_000017.9:g.43166097T>G NCBI36
NG_012166.1:g.5489T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.278T>G MANE Select ENSP00000177694.1:p.Phe93Cys
ENST00000177694.1:c.278T>G ENSP00000177694.1:p.Phe93Cys
ENST00000581328.1:n.308T>G
NM_013351.1:c.278T>G NP_037483.1:p.Phe93Cys
XM_011524698.1:c.278T>G XP_011523000.1:p.Phe93Cys
NM_013351.2:c.278T>G MANE Select NP_037483.1:p.Phe93Cys