Canonical Allele Identifier: CA2262810712

Gene: TBX21

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47744807T= , CM000679.2:g.47744807T=	GRCh38
NC_000017.10:g.45822173T= , CM000679.1:g.45822173T=	GRCh37
NC_000017.9:g.43177172T=	NCBI36
NG_012166.1:g.16564T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.1049T= MANE Select	ENSP00000177694.1:p.Leu350=
ENST00000177694.1:c.1049T=	ENSP00000177694.1:p.Leu350=
NM_013351.1:c.1049T=	NP_037483.1:p.Leu350=
XM_011524698.1:c.1112T=	XP_011523000.1:p.Leu371=
XM_011524699.1:c.716T=	XP_011523001.1:p.Leu239=
NM_013351.2:c.1049T= MANE Select	NP_037483.1:p.Leu350=