Canonical Allele Identifier: CA500449469
Gene: TBX21 HGNC NCBI

Linked Data

dbSNP Id: rs1432286629

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733478C>T , CM000679.2:g.47733478C>T GRCh38
NC_000017.10:g.45810844C>T , CM000679.1:g.45810844C>T GRCh37
NC_000017.9:g.43165843C>T NCBI36
NG_012166.1:g.5235C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.24C>T MANE Select ENSP00000177694.1:p.Cys8=
ENST00000177694.1:c.24C>T ENSP00000177694.1:p.Cys8=
ENST00000581328.1:n.54C>T
NM_013351.1:c.24C>T NP_037483.1:p.Cys8=
XM_011524698.1:c.24C>T XP_011523000.1:p.Cys8=
NM_013351.2:c.24C>T MANE Select NP_037483.1:p.Cys8=