Canonical Allele Identifier: CA400050510
Gene: TBX21 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.45822185A>G (hg19) chr17:g.47744819A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47744819A>G , CM000679.2:g.47744819A>G GRCh38
NC_000017.10:g.45822185A>G , CM000679.1:g.45822185A>G GRCh37
NC_000017.9:g.43177184A>G NCBI36
NG_012166.1:g.16576A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.1061A>G MANE Select ENSP00000177694.1:p.His354Arg
ENST00000177694.1:c.1061A>G ENSP00000177694.1:p.His354Arg
NM_013351.1:c.1061A>G NP_037483.1:p.His354Arg
XM_011524698.1:c.1124A>G XP_011523000.1:p.His375Arg
XM_011524699.1:c.728A>G XP_011523001.1:p.His243Arg
NM_013351.2:c.1061A>G MANE Select NP_037483.1:p.His354Arg
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