Canonical Allele Identifier: CA500450791

Gene: TBX21

Linked Data

• MyVariant Identifiers: chr17:g.45822159C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47744793C>G , CM000679.2:g.47744793C>G	GRCh38
NC_000017.10:g.45822159C>G , CM000679.1:g.45822159C>G	GRCh37
NC_000017.9:g.43177158C>G	NCBI36
NG_012166.1:g.16550C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.1035C>G MANE Select	ENSP00000177694.1:p.Pro345=
ENST00000177694.1:c.1035C>G	ENSP00000177694.1:p.Pro345=
NM_013351.1:c.1035C>G	NP_037483.1:p.Pro345=
XM_011524698.1:c.1098C>G	XP_011523000.1:p.Pro366=
XM_011524699.1:c.702C>G	XP_011523001.1:p.Pro234=
NM_013351.2:c.1035C>G MANE Select	NP_037483.1:p.Pro345=