Canonical Allele Identifier: CA400057652
Gene: TBX21 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733565C>A , CM000679.2:g.47733565C>A GRCh38
NC_000017.10:g.45810931C>A , CM000679.1:g.45810931C>A GRCh37
NC_000017.9:g.43165930C>A NCBI36
NG_012166.1:g.5322C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000177694.2:c.111C>A MANE Select ENSP00000177694.1:p.Tyr37Ter
ENST00000177694.1:c.111C>A ENSP00000177694.1:p.Tyr37Ter
ENST00000581328.1:n.141C>A
NM_013351.1:c.111C>A NP_037483.1:p.Tyr37Ter
XM_011524698.1:c.111C>A XP_011523000.1:p.Tyr37Ter
NM_013351.2:c.111C>A MANE Select NP_037483.1:p.Tyr37Ter