Canonical Allele Identifier: CA400059731
Gene: TBX21 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.45811262T>G (hg19) chr17:g.47733896T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733896T>G , CM000679.2:g.47733896T>G GRCh38
NC_000017.10:g.45811262T>G , CM000679.1:g.45811262T>G GRCh37
NC_000017.9:g.43166261T>G NCBI36
NG_012166.1:g.5653T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.442T>G MANE Select ENSP00000177694.1:p.Ser148Ala
ENST00000177694.1:c.442T>G ENSP00000177694.1:p.Ser148Ala
ENST00000581328.1:n.472T>G
NM_013351.1:c.442T>G NP_037483.1:p.Ser148Ala
XM_011524698.1:c.442T>G XP_011523000.1:p.Ser148Ala
NM_013351.2:c.442T>G MANE Select NP_037483.1:p.Ser148Ala
Search 100 bp 5'
Search 100 bp 3'