Canonical Allele Identifier: CA2262810689

Gene: TBX21

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47744734C= , CM000679.2:g.47744734C=	GRCh38
NC_000017.10:g.45822100C= , CM000679.1:g.45822100C=	GRCh37
NC_000017.9:g.43177099C=	NCBI36
NG_012166.1:g.16491C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.990-14C= MANE Select	ENSP00000177694.1:n.990-14C=
ENST00000177694.1:c.990-14C=	ENSP00000177694.1:n.990-14C=
NM_013351.1:c.990-14C=	NP_037483.1:n.990-14C=
XM_011524698.1:c.1053-14C=	XP_011523000.1:n.1053-14C=
XM_011524699.1:c.657-14C=	XP_011523001.1:n.657-14C=
NM_013351.2:c.990-14C= MANE Select	NP_037483.1:n.990-14C=