Canonical Allele Identifier: CA400058253
Gene: TBX21 HGNC NCBI

Linked Data

dbSNP Id: rs1174613256

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733657C>G , CM000679.2:g.47733657C>G GRCh38
NC_000017.10:g.45811023C>G , CM000679.1:g.45811023C>G GRCh37
NC_000017.9:g.43166022C>G NCBI36
NG_012166.1:g.5414C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.203C>G MANE Select ENSP00000177694.1:p.Pro68Arg
ENST00000177694.1:c.203C>G ENSP00000177694.1:p.Pro68Arg
ENST00000581328.1:n.233C>G
NM_013351.1:c.203C>G NP_037483.1:p.Pro68Arg
XM_011524698.1:c.203C>G XP_011523000.1:p.Pro68Arg
NM_013351.2:c.203C>G MANE Select NP_037483.1:p.Pro68Arg