Canonical Allele Identifier: CA2262805603

Gene: TBX21

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47733429T= , CM000679.2:g.47733429T=	GRCh38
NC_000017.10:g.45810795T= , CM000679.1:g.45810795T=	GRCh37
NC_000017.9:g.43165794T=	NCBI36
NG_012166.1:g.5186T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.-26T= MANE Select	ENSP00000177694.1:n.-26T=
ENST00000177694.1:c.-26T=	ENSP00000177694.1:n.-26T=
ENST00000581328.1:n.5T=
NM_013351.1:c.-26T=	NP_037483.1:n.-26T=
XM_011524698.1:c.-26T=	XP_011523000.1:n.-26T=
NM_013351.2:c.-26T= MANE Select	NP_037483.1:n.-26T=