Canonical Allele Identifier: CA400050784
Gene: TBX21 HGNC NCBI

Linked Data

dbSNP Id: rs1567921749

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47744848C>T , CM000679.2:g.47744848C>T GRCh38
NC_000017.10:g.45822214C>T , CM000679.1:g.45822214C>T GRCh37
NC_000017.9:g.43177213C>T NCBI36
NG_012166.1:g.16605C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.1090C>T MANE Select ENSP00000177694.1:p.Pro364Ser
ENST00000177694.1:c.1090C>T ENSP00000177694.1:p.Pro364Ser
NM_013351.1:c.1090C>T NP_037483.1:p.Pro364Ser
XM_011524698.1:c.1153C>T XP_011523000.1:p.Pro385Ser
XM_011524699.1:c.757C>T XP_011523001.1:p.Pro253Ser
NM_013351.2:c.1090C>T MANE Select NP_037483.1:p.Pro364Ser