Canonical Allele Identifier: CA2262805769

Gene: TBX21

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47733745G= , CM000679.2:g.47733745G=	GRCh38
NC_000017.10:g.45811111G= , CM000679.1:g.45811111G=	GRCh37
NC_000017.9:g.43166110G=	NCBI36
NG_012166.1:g.5502G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000177694.2:c.291G= MANE Select	ENSP00000177694.1:p.Ala97=
ENST00000177694.1:c.291G=	ENSP00000177694.1:p.Ala97=
ENST00000581328.1:n.321G=
NM_013351.1:c.291G=	NP_037483.1:p.Ala97=
XM_011524698.1:c.291G=	XP_011523000.1:p.Ala97=
NM_013351.2:c.291G= MANE Select	NP_037483.1:p.Ala97=