Canonical Allele Identifier: CA2262805831
Gene: TBX21 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733874G= , CM000679.2:g.47733874G= GRCh38
NC_000017.10:g.45811240G= , CM000679.1:g.45811240G= GRCh37
NC_000017.9:g.43166239G= NCBI36
NG_012166.1:g.5631G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.420G= MANE Select ENSP00000177694.1:p.Ala140=
ENST00000177694.1:c.420G= ENSP00000177694.1:p.Ala140=
ENST00000581328.1:n.450G=
NM_013351.1:c.420G= NP_037483.1:p.Ala140=
XM_011524698.1:c.420G= XP_011523000.1:p.Ala140=
NM_013351.2:c.420G= MANE Select NP_037483.1:p.Ala140=
Search 100 bp 5'
Search 100 bp 3'