Canonical Allele Identifier: CA400049901
Gene: TBX21 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.45822116T>A (hg19) chr17:g.47744750T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47744750T>A , CM000679.2:g.47744750T>A GRCh38
NC_000017.10:g.45822116T>A , CM000679.1:g.45822116T>A GRCh37
NC_000017.9:g.43177115T>A NCBI36
NG_012166.1:g.16507T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.992T>A MANE Select ENSP00000177694.1:p.Met331Lys
ENST00000177694.1:c.992T>A ENSP00000177694.1:p.Met331Lys
NM_013351.1:c.992T>A NP_037483.1:p.Met331Lys
XM_011524698.1:c.1055T>A XP_011523000.1:p.Met352Lys
XM_011524699.1:c.659T>A XP_011523001.1:p.Met220Lys
NM_013351.2:c.992T>A MANE Select NP_037483.1:p.Met331Lys
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