Canonical Allele Identifier: CA500450749

Gene: TBX21

Linked Data

• dbSNP Id: rs2032308896
• MyVariant Identifiers: chr17:g.45822147C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47744781C>T , CM000679.2:g.47744781C>T	GRCh38
NC_000017.10:g.45822147C>T , CM000679.1:g.45822147C>T	GRCh37
NC_000017.9:g.43177146C>T	NCBI36
NG_012166.1:g.16538C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.1023C>T MANE Select	ENSP00000177694.1:p.Ser341=
ENST00000177694.1:c.1023C>T	ENSP00000177694.1:p.Ser341=
NM_013351.1:c.1023C>T	NP_037483.1:p.Ser341=
XM_011524698.1:c.1086C>T	XP_011523000.1:p.Ser362=
XM_011524699.1:c.690C>T	XP_011523001.1:p.Ser230=
NM_013351.2:c.1023C>T MANE Select	NP_037483.1:p.Ser341=