Canonical Allele Identifier: CA984262674
Gene: TBX21 HGNC NCBI

Linked Data

dbSNP Id: rs2032161507

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733385C>T , CM000679.2:g.47733385C>T GRCh38
NC_000017.10:g.45810751C>T , CM000679.1:g.45810751C>T GRCh37
NC_000017.9:g.43165750C>T NCBI36
NG_012166.1:g.5142C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.-70C>T MANE Select ENSP00000177694.1:n.-70C>T
ENST00000177694.1:c.-70C>T ENSP00000177694.1:n.-70C>T
NM_013351.1:c.-70C>T NP_037483.1:n.-70C>T
XM_011524698.1:c.-70C>T XP_011523000.1:n.-70C>T
NM_013351.2:c.-70C>T MANE Select NP_037483.1:n.-70C>T