Canonical Allele Identifier: CA2262810715

Gene: TBX21

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47744810G= , CM000679.2:g.47744810G=	GRCh38
NC_000017.10:g.45822176G= , CM000679.1:g.45822176G=	GRCh37
NC_000017.9:g.43177175G=	NCBI36
NG_012166.1:g.16567G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.1052G= MANE Select	ENSP00000177694.1:p.Gly351=
ENST00000177694.1:c.1052G=	ENSP00000177694.1:p.Gly351=
NM_013351.1:c.1052G=	NP_037483.1:p.Gly351=
XM_011524698.1:c.1115G=	XP_011523000.1:p.Gly372=
XM_011524699.1:c.719G=	XP_011523001.1:p.Gly240=
NM_013351.2:c.1052G= MANE Select	NP_037483.1:p.Gly351=