Canonical Allele Identifier: CA400058775
Gene: TBX21 HGNC NCBI

Linked Data

gnomAD v4: 17-47733733-C-A
MyVariant Identifiers: chr17:g.45811099C>A (hg19) chr17:g.47733733C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733733C>A , CM000679.2:g.47733733C>A GRCh38
NC_000017.10:g.45811099C>A , CM000679.1:g.45811099C>A GRCh37
NC_000017.9:g.43166098C>A NCBI36
NG_012166.1:g.5490C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.279C>A MANE Select ENSP00000177694.1:p.Phe93Leu
ENST00000177694.1:c.279C>A ENSP00000177694.1:p.Phe93Leu
ENST00000581328.1:n.309C>A
NM_013351.1:c.279C>A NP_037483.1:p.Phe93Leu
XM_011524698.1:c.279C>A XP_011523000.1:p.Phe93Leu
NM_013351.2:c.279C>A MANE Select NP_037483.1:p.Phe93Leu
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