Canonical Allele Identifier: CA8626448
Gene: TBX21 HGNC NCBI

Linked Data

ClinVar Variation Id: 2230658
ClinVar RCV Id: RCV004097194
dbSNP Id: rs759136182

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47744821T>C , CM000679.2:g.47744821T>C GRCh38
NC_000017.10:g.45822187T>C , CM000679.1:g.45822187T>C GRCh37
NC_000017.9:g.43177186T>C NCBI36
NG_012166.1:g.16578T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.1063T>C MANE Select ENSP00000177694.1:p.Tyr355His
ENST00000177694.1:c.1063T>C ENSP00000177694.1:p.Tyr355His
NM_013351.1:c.1063T>C NP_037483.1:p.Tyr355His
XM_011524698.1:c.1126T>C XP_011523000.1:p.Tyr376His
XM_011524699.1:c.730T>C XP_011523001.1:p.Tyr244His
NM_013351.2:c.1063T>C MANE Select NP_037483.1:p.Tyr355His