Canonical Allele Identifier: CA400058827
Gene: TBX21 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.45811118G>T (hg19) chr17:g.47733752G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733752G>T , CM000679.2:g.47733752G>T GRCh38
NC_000017.10:g.45811118G>T , CM000679.1:g.45811118G>T GRCh37
NC_000017.9:g.43166117G>T NCBI36
NG_012166.1:g.5509G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000177694.2:c.298G>T MANE Select ENSP00000177694.1:p.Glu100Ter
ENST00000177694.1:c.298G>T ENSP00000177694.1:p.Glu100Ter
ENST00000581328.1:n.328G>T
NM_013351.1:c.298G>T NP_037483.1:p.Glu100Ter
XM_011524698.1:c.298G>T XP_011523000.1:p.Glu100Ter
NM_013351.2:c.298G>T MANE Select NP_037483.1:p.Glu100Ter
Search 100 bp 5'
Search 100 bp 3'