Canonical Allele Identifier: CA400050195
Gene: TBX21 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47744782C>T , CM000679.2:g.47744782C>T GRCh38
NC_000017.10:g.45822148C>T , CM000679.1:g.45822148C>T GRCh37
NC_000017.9:g.43177147C>T NCBI36
NG_012166.1:g.16539C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.1024C>T MANE Select ENSP00000177694.1:p.Pro342Ser
ENST00000177694.1:c.1024C>T ENSP00000177694.1:p.Pro342Ser
NM_013351.1:c.1024C>T NP_037483.1:p.Pro342Ser
XM_011524698.1:c.1087C>T XP_011523000.1:p.Pro363Ser
XM_011524699.1:c.691C>T XP_011523001.1:p.Pro231Ser
NM_013351.2:c.1024C>T MANE Select NP_037483.1:p.Pro342Ser