Canonical Allele Identifier: CA2262805725

Gene: TBX21

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47733648C= , CM000679.2:g.47733648C=	GRCh38
NC_000017.10:g.45811014C= , CM000679.1:g.45811014C=	GRCh37
NC_000017.9:g.43166013C=	NCBI36
NG_012166.1:g.5405C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.194C= MANE Select	ENSP00000177694.1:p.Pro65=
ENST00000177694.1:c.194C=	ENSP00000177694.1:p.Pro65=
ENST00000581328.1:n.224C=
NM_013351.1:c.194C=	NP_037483.1:p.Pro65=
XM_011524698.1:c.194C=	XP_011523000.1:p.Pro65=
NM_013351.2:c.194C= MANE Select	NP_037483.1:p.Pro65=