Canonical Allele Identifier: CA400050585
Gene: TBX21 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47744827C>G , CM000679.2:g.47744827C>G GRCh38
NC_000017.10:g.45822193C>G , CM000679.1:g.45822193C>G GRCh37
NC_000017.9:g.43177192C>G NCBI36
NG_012166.1:g.16584C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.1069C>G MANE Select ENSP00000177694.1:p.Pro357Ala
ENST00000177694.1:c.1069C>G ENSP00000177694.1:p.Pro357Ala
NM_013351.1:c.1069C>G NP_037483.1:p.Pro357Ala
XM_011524698.1:c.1132C>G XP_011523000.1:p.Pro378Ala
XM_011524699.1:c.736C>G XP_011523001.1:p.Pro246Ala
NM_013351.2:c.1069C>G MANE Select NP_037483.1:p.Pro357Ala