Canonical Allele Identifier: CA400058276
Gene: TBX21 HGNC NCBI

Linked Data

gnomAD v4: 17-47733660-G-T
MyVariant Identifiers: chr17:g.45811026G>T (hg19) chr17:g.47733660G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733660G>T , CM000679.2:g.47733660G>T GRCh38
NC_000017.10:g.45811026G>T , CM000679.1:g.45811026G>T GRCh37
NC_000017.9:g.43166025G>T NCBI36
NG_012166.1:g.5417G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.206G>T MANE Select ENSP00000177694.1:p.Ser69Ile
ENST00000177694.1:c.206G>T ENSP00000177694.1:p.Ser69Ile
ENST00000581328.1:n.236G>T
NM_013351.1:c.206G>T NP_037483.1:p.Ser69Ile
XM_011524698.1:c.206G>T XP_011523000.1:p.Ser69Ile
NM_013351.2:c.206G>T MANE Select NP_037483.1:p.Ser69Ile
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