Canonical Allele Identifier: CA500450912

Gene: TBX21

Linked Data

• MyVariant Identifiers: chr17:g.45822195T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47744829T>A , CM000679.2:g.47744829T>A	GRCh38
NC_000017.10:g.45822195T>A , CM000679.1:g.45822195T>A	GRCh37
NC_000017.9:g.43177194T>A	NCBI36
NG_012166.1:g.16586T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.1071T>A MANE Select	ENSP00000177694.1:p.Pro357=
ENST00000177694.1:c.1071T>A	ENSP00000177694.1:p.Pro357=
NM_013351.1:c.1071T>A	NP_037483.1:p.Pro357=
XM_011524698.1:c.1134T>A	XP_011523000.1:p.Pro378=
XM_011524699.1:c.738T>A	XP_011523001.1:p.Pro246=
NM_013351.2:c.1071T>A MANE Select	NP_037483.1:p.Pro357=