Canonical Allele Identifier: CA2262805841
Gene: TBX21 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733919A= , CM000679.2:g.47733919A= GRCh38
NC_000017.10:g.45811285A= , CM000679.1:g.45811285A= GRCh37
NC_000017.9:g.43166284A= NCBI36
NG_012166.1:g.5676A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.465A= MANE Select ENSP00000177694.1:p.Thr155=
ENST00000177694.1:c.465A= ENSP00000177694.1:p.Thr155=
ENST00000581328.1:n.495A=
NM_013351.1:c.465A= NP_037483.1:p.Thr155=
XM_011524698.1:c.465A= XP_011523000.1:p.Thr155=
NM_013351.2:c.465A= MANE Select NP_037483.1:p.Thr155=
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