Canonical Allele Identifier: CA2638459062
Gene: TBX21 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733363C>A , CM000679.2:g.47733363C>A GRCh38
NC_000017.10:g.45810729C>A , CM000679.1:g.45810729C>A GRCh37
NC_000017.9:g.43165728C>A NCBI36
NG_012166.1:g.5120C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.-92C>A MANE Select ENSP00000177694.1:n.-92C>A
ENST00000177694.1:c.-92C>A ENSP00000177694.1:n.-92C>A
NM_013351.1:c.-92C>A NP_037483.1:n.-92C>A
XM_011524698.1:c.-92C>A XP_011523000.1:n.-92C>A
NM_013351.2:c.-92C>A MANE Select NP_037483.1:n.-92C>A