Canonical Allele Identifier: CA2262810705

Gene: TBX21

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47744783C= , CM000679.2:g.47744783C=	GRCh38
NC_000017.10:g.45822149C= , CM000679.1:g.45822149C=	GRCh37
NC_000017.9:g.43177148C=	NCBI36
NG_012166.1:g.16540C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.1025C= MANE Select	ENSP00000177694.1:p.Pro342=
ENST00000177694.1:c.1025C=	ENSP00000177694.1:p.Pro342=
NM_013351.1:c.1025C=	NP_037483.1:p.Pro342=
XM_011524698.1:c.1088C=	XP_011523000.1:p.Pro363=
XM_011524699.1:c.692C=	XP_011523001.1:p.Pro231=
NM_013351.2:c.1025C= MANE Select	NP_037483.1:p.Pro342=