Canonical Allele Identifier: CA400050653
Gene: TBX21 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.45822202C>A (hg19) chr17:g.47744836C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47744836C>A , CM000679.2:g.47744836C>A GRCh38
NC_000017.10:g.45822202C>A , CM000679.1:g.45822202C>A GRCh37
NC_000017.9:g.43177201C>A NCBI36
NG_012166.1:g.16593C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.1078C>A MANE Select ENSP00000177694.1:p.Pro360Thr
ENST00000177694.1:c.1078C>A ENSP00000177694.1:p.Pro360Thr
NM_013351.1:c.1078C>A NP_037483.1:p.Pro360Thr
XM_011524698.1:c.1141C>A XP_011523000.1:p.Pro381Thr
XM_011524699.1:c.745C>A XP_011523001.1:p.Pro249Thr
NM_013351.2:c.1078C>A MANE Select NP_037483.1:p.Pro360Thr
Search 100 bp 5'
Search 100 bp 3'