Canonical Allele Identifier: CA400058767
Gene: TBX21 HGNC NCBI

Linked Data

gnomAD v4: 17-47733731-T-C
MyVariant Identifiers: chr17:g.45811097T>C (hg19) chr17:g.47733731T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733731T>C , CM000679.2:g.47733731T>C GRCh38
NC_000017.10:g.45811097T>C , CM000679.1:g.45811097T>C GRCh37
NC_000017.9:g.43166096T>C NCBI36
NG_012166.1:g.5488T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.277T>C MANE Select ENSP00000177694.1:p.Phe93Leu
ENST00000177694.1:c.277T>C ENSP00000177694.1:p.Phe93Leu
ENST00000581328.1:n.307T>C
NM_013351.1:c.277T>C NP_037483.1:p.Phe93Leu
XM_011524698.1:c.277T>C XP_011523000.1:p.Phe93Leu
NM_013351.2:c.277T>C MANE Select NP_037483.1:p.Phe93Leu
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