Canonical Allele Identifier: CA400050728
Gene: TBX21 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.45822208C>A (hg19) chr17:g.47744842C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47744842C>A , CM000679.2:g.47744842C>A GRCh38
NC_000017.10:g.45822208C>A , CM000679.1:g.45822208C>A GRCh37
NC_000017.9:g.43177207C>A NCBI36
NG_012166.1:g.16599C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.1084C>A MANE Select ENSP00000177694.1:p.Gln362Lys
ENST00000177694.1:c.1084C>A ENSP00000177694.1:p.Gln362Lys
NM_013351.1:c.1084C>A NP_037483.1:p.Gln362Lys
XM_011524698.1:c.1147C>A XP_011523000.1:p.Gln383Lys
XM_011524699.1:c.751C>A XP_011523001.1:p.Gln251Lys
NM_013351.2:c.1084C>A MANE Select NP_037483.1:p.Gln362Lys
Search 100 bp 5'
Search 100 bp 3'