Canonical Allele Identifier: CA2262805819
Gene: TBX21 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733838C= , CM000679.2:g.47733838C= GRCh38
NC_000017.10:g.45811204C= , CM000679.1:g.45811204C= GRCh37
NC_000017.9:g.43166203C= NCBI36
NG_012166.1:g.5595C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.384C= MANE Select ENSP00000177694.1:p.Pro128=
ENST00000177694.1:c.384C= ENSP00000177694.1:p.Pro128=
ENST00000581328.1:n.414C=
NM_013351.1:c.384C= NP_037483.1:p.Pro128=
XM_011524698.1:c.384C= XP_011523000.1:p.Pro128=
NM_013351.2:c.384C= MANE Select NP_037483.1:p.Pro128=
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