Canonical Allele Identifier: CA400058462
Gene: TBX21 HGNC NCBI

Linked Data

gnomAD v4: 17-47733684-A-T
MyVariant Identifiers: chr17:g.45811050A>T (hg19) chr17:g.47733684A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733684A>T , CM000679.2:g.47733684A>T GRCh38
NC_000017.10:g.45811050A>T , CM000679.1:g.45811050A>T GRCh37
NC_000017.9:g.43166049A>T NCBI36
NG_012166.1:g.5441A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.230A>T MANE Select ENSP00000177694.1:p.Tyr77Phe
ENST00000177694.1:c.230A>T ENSP00000177694.1:p.Tyr77Phe
ENST00000581328.1:n.260A>T
NM_013351.1:c.230A>T NP_037483.1:p.Tyr77Phe
XM_011524698.1:c.230A>T XP_011523000.1:p.Tyr77Phe
NM_013351.2:c.230A>T MANE Select NP_037483.1:p.Tyr77Phe
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