Canonical Allele Identifier: CA500652715

Gene: TBX21

Linked Data

• MyVariant Identifiers: chr17:g.45811186T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47733820T>G , CM000679.2:g.47733820T>G	GRCh38
NC_000017.10:g.45811186T>G , CM000679.1:g.45811186T>G	GRCh37
NC_000017.9:g.43166185T>G	NCBI36
NG_012166.1:g.5577T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.366T>G MANE Select	ENSP00000177694.1:p.Arg122=
ENST00000177694.1:c.366T>G	ENSP00000177694.1:p.Arg122=
ENST00000581328.1:n.396T>G
NM_013351.1:c.366T>G	NP_037483.1:p.Arg122=
XM_011524698.1:c.366T>G	XP_011523000.1:p.Arg122=
NM_013351.2:c.366T>G MANE Select	NP_037483.1:p.Arg122=