Canonical Allele Identifier: CA400059963
Gene: TBX21 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733929A>T , CM000679.2:g.47733929A>T GRCh38
NC_000017.10:g.45811295A>T , CM000679.1:g.45811295A>T GRCh37
NC_000017.9:g.43166294A>T NCBI36
NG_012166.1:g.5686A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.475A>T MANE Select ENSP00000177694.1:p.Ile159Phe
ENST00000177694.1:c.475A>T ENSP00000177694.1:p.Ile159Phe
ENST00000581328.1:n.505A>T
NM_013351.1:c.475A>T NP_037483.1:p.Ile159Phe
XM_011524698.1:c.475A>T XP_011523000.1:p.Ile159Phe
NM_013351.2:c.475A>T MANE Select NP_037483.1:p.Ile159Phe